journal article·2018-09

Ultra‐Light and Scalable Composite Lattice Materials

Christine E. Gregg, Joseph H. Kim, Kenneth C. Cheung

Advanced Engineering Materials· Volume 20· Issue 9
Publisher page

Abstract

Architected lattice materials are some of the stiffest and strongest materials at ultra‐light density (<10 mg cm−3), but scalable manufacturing with high‐performance constituent materials remains a challenge that limits their widespread adoption in load‐bearing applications. We show mesoscale, ultra‐light (5.8 mg cm−3) fiber‐reinforced polymer composite lattice structures that are reversibly assembled from building blocks manufactured with a best‐practice high‐precision, high‐repeatability, and high‐throughput process: injection molding. Chopped glass fiber‐reinforced polymer (polyetherimide) lattice materials produced with this method display absolute stiffness (8.41 MPa) and strength (19 kPa) typically associated with metallic hollow strut microlattices at similar mass density. Additional benefits such as strain recovery, discrete damage repair with recovery of original stiffness and strength, and ease of modeling are demonstrated.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Cellular and Composite Structures · Advanced Materials and Mechanics · Polymer composites and self-healing

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Mechanical Engineering, University of California Berkeley Berkeley CA 94720 USA

NASA Ames Research Center, Moffett Field CA 94035 USA

Funding

NASA Space Technologies Research Fellowship · NXX16AM65H · NASA ARMD Convergent Aerospace Solutions · NASA STMD Game Changing Development programs

References (25)

Show source-provided references
1. Arnold S. M. · Introd. to Aerosp. Mater · 2012 · 569
2. 10.1111/j.1551-2916.2011.04599.x10.1111/j.1551-2916.2011.04599.x ↗
3. 10.1007/BF0264554610.1007/BF02645546 ↗
4. 10.1016/S1359-6454(00)00379-710.1016/S1359-6454(00)00379-7 ↗
5. 10.1038/srep1382510.1038/srep13825 ↗
6. 10.1002/adma.20120453010.1002/adma.201204530 ↗
7. 10.1126/science.125229110.1126/science.1252291 ↗
8. 10.1038/nature1614510.1038/nature16145 ↗
9. 10.1038/srep2487110.1038/srep24871 ↗
10. 10.1002/adma.20140180410.1002/adma.201401804 ↗
11. 10.1126/science.121164910.1126/science.1211649 ↗
12. 10.1126/science.125590810.1126/science.1255908 ↗
13. 10.1016/j.matdes.2016.01.14610.1016/j.matdes.2016.01.146 ↗
14. 10.1126/science.124088910.1126/science.1240889 ↗
15. 10.1016/j.ijsolstr.2015.02.02010.1016/j.ijsolstr.2015.02.020 ↗
16. 10.1016/j.compscitech.2015.09.02210.1016/j.compscitech.2015.09.022 ↗
17. 10.1016/j.matdes.2016.03.08810.1016/j.matdes.2016.03.088 ↗
18. 10.1017/CBO978113987832610.1017/CBO9781139878326 ↗
19. 10.1016/j.jmps.2017.02.00210.1016/j.jmps.2017.02.002 ↗
20. 10.1016/j.actamat.2004.09.02410.1016/j.actamat.2004.09.024 ↗
21. 10.1126/sciadv.160153610.1126/sciadv.1601536 ↗
22. 10.1038/srep0211710.1038/srep02117 ↗
23. 10.1016/j.carbon.2015.01.00310.1016/j.carbon.2015.01.003 ↗
24. 10.1002/adma.20120457610.1002/adma.201204576 ↗
25. 10.1063/1.308629310.1063/1.3086293 ↗