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Minimise thermo-mechanical batch variations when processing medical grade lactide based copolymers in additive manufacturing

机译:在添加剂制造中加工医疗级丙交酯的共聚物时,最小化热机械批量变化

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摘要

Additive manufacturing is suitable for producing complex geometries; however, variation in thermo-mechanical properties is observed during one batch cycle when degradable aliphatic polyesters are used in melt extrusion-based methods. This is one important reason for why additive manufacturing has not yet been fully utilised to produce degradable medical implants. Herein, the internal variation has been minimised during one batch cycle by assessing the effect of different processing parameters when using commercially available medical grade copolymers. To minimise the molar mass, thermal and mechanical variation within one batch cycle, the rheologi-cal fingerprint of the commercially available medical grade poly(L-lactide-co-ε- caprolactone) and poly(L-lactide-co-trimethylene carbonate) has been correlated to the process parameters of the ARBURG Plastic Freeforming. An increase in the temperature up to 220°C and the associated increase in pressure are beneficial for the viscoelastic and thermally stable poly(L-lactide-co-ε-caprolactone). In contrast, a temperature below 220°C should be used for the poly(L-lactide-co-trimethylene carbonate) to reduce the variation in strain at break during one batch cycle. The residence time is decreased through the increase of the discharge parameter. An increase in temperature is however required to reduce the viscosity of the polymer and allow the pressure to stay within the machine limitations at higher discharge parameters. The results are highly relevant to the development of additive manufacturing for the production of degradable medical devices with identical properties. In fact, Food and Drug Administration guidelines for additive manufacturing of medical implants specify the need to control changes in for example material properties during the process.
机译:添加剂制造适用于生产复杂的几何形状;然而,当在熔融挤出基方法中使用可降解的脂族聚酯时,在一种批量循环期间观察到热机械性能的变化。这是为什么添加添加剂制造尚未充分利用以产生可降解的医疗植入物的一个重要原因。这里,通过在使用市售的医疗等级共聚物时评估不同加工参数的效果,在一个批次循环期间已经最小化内部变化。为了使一批循环内的摩尔质量,热量和机械变化最小化,市售的商业级聚(L-丙交酯 - 共ε-己内酯)和聚(L-丙交酯 - 共三甲基碳酸酯)的流变晶型指纹已经与Arburg塑料自由的过程参数相关联。在温度高达220℃的增加和压力的相应增加是针对粘弹性和热稳定的聚(L-丙交酯 - 共 - ε - 己内酯)是有益的。相反,低于220℃的温度应用于聚(L-丙交酯 - 共聚碳酸亚甲基酯),以减少一个批次循环期间断裂菌株的变化。通过放电参数的增加降低了停留时间。然而,温度的增加是为了降低聚合物的粘度并使压力保持在较高放电参数的机器限制内。结果与生产具有相同性质的可降解医用装置的添加剂制造的发展高度相关。事实上,食品和药物管理指南用于医疗植入物的添加剂制造规定了在该过程中控制例如材料特性的变化。

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