中国塑料 ›› 2018, Vol. 32 ›› Issue (11): 19-23,60.DOI: 10.19491/j.issn.1001-9278.2018.11.003

• 材料与性能 • 上一篇    下一篇

TPU对ABS熔融沉积成型性能的影响

池哲明1,2,夏新曙2,杨松伟2,纪锡辉1,2,陈庆华2,肖荔人1,2*   

  1. 1. 福建师范大学化学与材料学院
    2. 福建省污染控制与资源循环利用重点实验室

  • 收稿日期:2018-04-11 修回日期:2018-06-28 出版日期:2018-11-26 发布日期:2018-12-24
  • 基金资助:
    国家重点研发专项(2016YFB0302300);福建师范大学泉港石化研究院专项资金项目(2016YJY20)

Effect of TPU on Fused Deposition Modeling Performance of ABS/TPU Compounds

  • Received:2018-04-11 Revised:2018-06-28 Online:2018-11-26 Published:2018-12-24

摘要: 采用熔融共混制备丙烯腈-丁二烯-苯乙烯共聚物/热塑性聚氨酯(ABS/TPU)3D打印耗材,通过熔融沉积成型(FDM)制备标准测试样条,并对ABS/TPU体系的成型性能、力学性能、微观结构、流变性能进行研究。结果表明,TPU改性ABS的成型性能均优于未改性ABS,当TPU质量分数大于20 %时,成型过程不发生翘曲收缩现象;同时有较好的力学性能,缺口冲击强度为18.81 kJ/m2比纯ABS提高了95.94 %,拉伸强度为32.92 MPa,下降了8.5 %;TPU质量分数大于20 %时,材料发生韧性断裂,并随TPU的增加,断面粗糙程度增加,有空洞现象;ABS/TPU具有较好的相容性,且随TPU含量增加,ABS/TPU分子链扩散能力增加。

Abstract: The 3D printing filaments based on ABS/thermoplastic polyurethane (TPU) blends were prepared by a melt blending method. These 3D printing filaments were subsequently processed to the standard test samples by fused deposition modeling (FDM), and their modeling performance, mechanical properties, microstructure and rheological properties were investigated. The results indicted that the introduction of TPU improved the modeling performance of ABS. With the addition of 20 wt % of TPU into ABS, the warp shrinkage disappeared in the modeling process. At this weight fraction, the molded sample obtained the enhanced notched impact strength of 18.81 kJ/m2 and the declined tensile strength of 32.92 MPa, which increased by 95.94 % and decreased by 8.5 %, respectively, compared to those of pure ABS. Morphological observation indicated that the molded sample presented ductile fracture at a weight fraction of TPU over 20 wt %. Moreover, the roughness of the impact fracture surface with an increase of TPU content and some holes were observed. The rheological investigation indicated that there was good compatibility between ABS and TPU, and the increase of TPU content enhanced the diffusion capability of macromolecular chains for these two polymers.