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丙交酯开环法合成聚乳酸工艺探讨 总被引:6,自引:1,他引:5
研究了丙交酯开环法合成聚乳酸的工艺路线,考察了反应温度、反应时间、催化剂用量等工艺条件对聚乳酸分子质量的影响,在优化工艺条件下可以得到高分子质量和高结晶度的聚乳酸。 相似文献
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生物降解材料聚乳酸的合成 总被引:18,自引:0,他引:18
系统地介绍了包括丙交酯二步法、乳酸溶液聚合法和乳酸熔融聚合法在内的各种聚乳酸合成方法;并从安全和经济的观点出发,对聚乳酸的合成研究方向进行了展望,指出使用安全无毒的催化剂进行乳酸直接熔融聚合生产聚乳酸尤其值得大力开发。 相似文献
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以D,L乳酸为原料、ZnO为催化剂,制备中间体丙交酯;再以丙交酯为原料、ZnO为催化剂,开环制得了较高相对分子质量的聚乳酸。用红外光谱仪(IR)对丙交酯及聚乳酸进行了表征,并讨论了影响丙交酯产率、聚乳酸相对分子质量的主要因素。得出在压力1.7×104Pa、催化剂质量分数为2.2%的条件下,两步脱水后制得的丙交酯经多次纯化后,其最大产率可达31%。在压力1.7×104Pa、催化剂质量分数0.06%时,可得到相对分子质量为1.1×105的聚乳酸。 相似文献
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Arianna Zanoni Flavio Tollini Cora Casiraghi Giuseppe Storti Mattia Sponchioni Davide Moscatelli 《加拿大化工杂志》2023,101(9):4845-4859
Engineered polylactic acid (PLA) nanoparticles synthesized from oligo(lactic acid) macromonomers have been studied over the last decades for controlled drug delivery. These macromonomers are typically produced via ring-opening polymerization (ROP) of the cyclic dimer lactide, initiated by 2-hydroxyethyl methacrylate (HEMA). This reaction route, despite leading to well-defined macromonomers, relies on the production of lactide from lactic acid, which burdens the ROP overall cost for more than 30%. In this work, we report the synthesis of PLA-based macromonomers by direct polycondensation of lactic acid in the presence of HEMA as a valuable alternative to ROP. In particular, we compare the two processes side by side, focusing on the production of three HEMA-LAn macromonomers, with n = 2, 4, and 6. Detailed kinetic models are developed for both reaction systems, and the corresponding parameters are estimated by fitting the experimental data. Through these models, the reaction kinetics as well as the time evolution of the entire chain length distributions of the products from polycondensation and ROP could be reliably predicted. This way, we demonstrated that polycondensation is a valuable alternative to ROP only for macromonomers with an average chain length of up to 4 and that ROP remains the main route to longer chains, when a strict control over the chain length distribution is required. 相似文献
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Poly(tetramethylene ether glycol) (PTMG), widely used as a precursor in the fabrication of commodity polymers, is typically produced byacid-catalyzed polymerization of tetrahydrofuran (THF). Herein, we report a detailed investigation of the cationic ring-opening polymerization of THF catalyzed by ferric chloride (FeCl3), which can be considered as a strong Lewisacid. The polymerization reactions were performed in the presence of acetic anhydride at 20°C with FeCl3, which readily produced poly(tetramethylene ether glycol diester) (PTMG_DE). A maximum yield of 79.2% was obtained within 30 min using a FeCl3 to acetic anhydride molar ratio of 5:4. The resulting polymers generally exhibited low molecular weights and a narrow polydispersity index and could be easily converted into PTMG using aqueous NaOH. In contrast with the FeCl3-acetic anhydride system, other iron-based catalysts such as FeCl2 and FeCl3·6H2O did not show any noticeable activity in the polymerization of THF. The proposed mechanism involves initiation of the acetyl cation generated by FeCl3, propagation by nucleophilic addition of THF, and termination by the acetate anion, accounting for the high activity of the FeCl3 catalyst for THF polymerization. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47999. 相似文献
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聚乳酸中间体——丙交酯制备工艺 总被引:1,自引:0,他引:1
研究了间接法合成聚乳酸用的中间体丙交酯的制备工艺。以工业D,L-乳酸(lacticacid)为原料,丙交酯粗产物的收率为考查指标,通过正交实验得到了最佳制备工艺条件为:以4%(v/v)的辛酸亚锡为催化剂,脱水温度为180℃,解聚温度为285℃,得到粗产物收率为72.4%。粗品丙交酯1次重结晶后收率为59.3%,熔点为95.0~96.2℃;5次重结晶后总收率为50.7%,熔点为125.2~126.5℃。同时采用FTIR与1HNMR对产物进行了结构表征。 相似文献
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Radical emulsion polymerizations of vinylcyclopropanes, 1,1-bis(ethoxycarbonyl)-2-vinylcyclopropane (ECVCP) and 1,1-dichloro-2-vinylcyclopropane (CVCP) were examined. ECVCP underwent soap-free and soap-in emulsion polymerizations satisfactorily to afford the ring-opened polymer in good yields. Polymer emulsions were obtained in a spherical shape with single particle size distribution. Meanwhile, emulsion polymerization of CVCP proceeded in only a low conversion. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 497–501, 1998 相似文献
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Julian Chojnowski Krystyna Rózga 《Journal of Inorganic and Organometallic Polymers》1992,2(3):297-317
Six-membered ring siloxane monomers
containing a phosphorus electron-donating groupR=–CH2CH2PPh2 (1), –CH2CH2P(S)Ph2 (2), and –CH2CH2P(O)Ph2 (3) were synthesized. The anionic ring-opening polymerization of these monomers with kinetic control of products has been studied using tetrahydrofuran (THF) as solvent and lithium silanolates as initiators. The polymerization leads to a high molecular weight linear polymer with a very good yield in the case of2 and with a fairly good yield in the case of1 and3. The presence of the phosphorus group enhances the cyclization and broadens the molecular weight distribution of the linear polymer. This effect is relatively weak for the thiophosphinoyl group. At least in the case of the polymer obtained from2, phosphorus groups are distributed uniformly in the macromolecule, however, their arrangement along the chain is not regular. The interaction of polymers obtained from monomers1, 2, and3 with some electrophiles such as alkyl or silyl halides was demonstrated to lead to generation of polyelectrolytes. 相似文献
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This paper reviews the recent discoveries that were achieved by our group in the field of particle synthesis via ring-opening metathesis polymerization (ROMP). Both polynorbornene and polybutadiene-based particles were prepared by the respective ROMP of norbornene and cyclooctadiene initiated by (PCy3)2Cl2RuCHPh using several methods of polymerization in dispersed media, such as dispersion, suspension and miniemulsion. Depending upon the process implemented, particles size was found to range from 300 nm to 20 μm. 相似文献