TY - JOUR
T1 - Hierarchical Mechanisms of Lateral Interactions in High-Performance Fibers
AU - Stockdale, Taylor A.
AU - Cole, Daniel P.
AU - Staniszewski, Jeffrey M.
AU - Roenbeck, Michael R.
AU - Papkov, Dimitry
AU - Lustig, Steve R.
AU - Dzenis, Yuris A.
AU - Strawhecker, Kenneth E.
N1 - Funding Information:
T.A.S. and Y.A.D. acknowledge the partial support of this work by the grants from National Science Foundation (Division of Material Research-1310534, Civil, Mechanical, and Manufacturing Innovation-1463636), Office of Naval Research (N000141410663), National Institute of Health (1R01HL125736-01), and Nebraska Center for Energy Science Research. Characterization and analysis were performed in part in the Nebraska Nanoscale Facility: National Nanotechnology Coordinated Infrastructure and the Nebraska Center for Materials and Nanoscience (and/or the NanoEngineering Research Core Facility (NERCF)), which are supported by the National Science Foundation under Award ECCS: 1542182, and the Nebraska Research Initiative. The authors thank the U.S. Army Natick Soldier Research, Development and Engineering Center for supplying the ballistic fibers used in this study. Research was sponsored in part by the Army Research Laboratory and was accomplished under Cooperative Agreement Numbers W911NF-16-2-0008 and W911NF-18-2-0273. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed implied, of the United States Merchant Marine Academy, the U.S. Department of Transportation, the Army Research Laboratory or the U.S. Government. The U.S. Government is authorized to reproduce and distribute reprints for Government purposes notwithstanding any copyright notation herein.
Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/5/13
Y1 - 2020/5/13
N2 - The processing conditions used in the production of advanced polymer fibers facilitate the formation of an oriented fibrillar network that consists of structures spanning multiple length scales. The irregular nature of fiber tensile fracture surfaces suggests that their structural integrity is defined by the degree of lateral (interfacial) interactions that exist within the fiber microstructure. To date, experimental studies have quantified interfacial adhesion between nanoscale fibrils measuring 10-50 nm in width, and the global fracture energy through applying peel loads to fiber halves. However, a more in-depth evaluation of tensile fracture indicates that fiber failure typically occurs at an intermediate length scale, involving fibrillation along interfaces between fibril bundles of a few 100s of nanometers in width. Interaction mechanisms at this length scale have not yet been studied, due in part to a lack of established experimental techniques. Here, a new focused ion beam-based sample preparation protocol is combined with nanoindentation to probe interfaces at the intermediate length scale in two high-performance fibers, a rigid-rod poly(p-phenylene terephthalamide) and a flexible chain ultrahigh molecular weight polyethylene fiber. Higher interfacial separation energy recorded in the rigid-rod fiber correlated with less intensive fibrillation during failure and is discussed in the context of fiber chemistry and processing. Power law scaling of the total absorbed interfacial separation energy at three different scales in the polyethylene fiber is observed and analyzed, and distinct energy absorption mechanisms, featuring a degree of self-similarity, are identified. The contribution of these mechanisms to the overall integrity of the fiber is discussed, and the importance of the intermediate scale is elucidated. Results from this study provide new insights into the mechanical implications of hierarchical lateral interactions and will aid in the development of novel fibers with further improved mechanical performance.
AB - The processing conditions used in the production of advanced polymer fibers facilitate the formation of an oriented fibrillar network that consists of structures spanning multiple length scales. The irregular nature of fiber tensile fracture surfaces suggests that their structural integrity is defined by the degree of lateral (interfacial) interactions that exist within the fiber microstructure. To date, experimental studies have quantified interfacial adhesion between nanoscale fibrils measuring 10-50 nm in width, and the global fracture energy through applying peel loads to fiber halves. However, a more in-depth evaluation of tensile fracture indicates that fiber failure typically occurs at an intermediate length scale, involving fibrillation along interfaces between fibril bundles of a few 100s of nanometers in width. Interaction mechanisms at this length scale have not yet been studied, due in part to a lack of established experimental techniques. Here, a new focused ion beam-based sample preparation protocol is combined with nanoindentation to probe interfaces at the intermediate length scale in two high-performance fibers, a rigid-rod poly(p-phenylene terephthalamide) and a flexible chain ultrahigh molecular weight polyethylene fiber. Higher interfacial separation energy recorded in the rigid-rod fiber correlated with less intensive fibrillation during failure and is discussed in the context of fiber chemistry and processing. Power law scaling of the total absorbed interfacial separation energy at three different scales in the polyethylene fiber is observed and analyzed, and distinct energy absorption mechanisms, featuring a degree of self-similarity, are identified. The contribution of these mechanisms to the overall integrity of the fiber is discussed, and the importance of the intermediate scale is elucidated. Results from this study provide new insights into the mechanical implications of hierarchical lateral interactions and will aid in the development of novel fibers with further improved mechanical performance.
KW - fibrillar network
KW - high-performance fiber
KW - mechanical properties
KW - processing
KW - structure
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U2 - 10.1021/acsami.9b23459
DO - 10.1021/acsami.9b23459
M3 - Article
C2 - 32142249
AN - SCOPUS:85084694447
SN - 1944-8244
VL - 12
SP - 22256
EP - 22267
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 19
ER -