TY - JOUR
T1 - Reactive Compression Molding Post-Inverse Vulcanization
T2 - A Method to Assemble, Recycle, and Repurpose Sulfur Polymers and Composites
AU - Lundquist, Nicholas A.
AU - Tikoalu, Alfrets D.
AU - Worthington, Max J.H.
AU - Shapter, Ryan
AU - Tonkin, Samuel J.
AU - Stojcevski, Filip
AU - Mann, Maximilian
AU - Gibson, Christopher T.
AU - Gascooke, Jason R.
AU - Karton, Amir
AU - Henderson, Luke C.
AU - Esdaile, Louisa J.
AU - Chalker, Justin M.
N1 - Funding Information:
The authors acknowledge financial support from the Australian Research Council (DP200100090), The AMP Tomorrow Fund and the Flinders University Impact Seed Funding for Early Career Researchers (J.M.C.). The authors also acknowledge the support of the Microscopy Australia research facility at Flinders University. This work was performed in part at the South Australian node of the Australian National Fabrication Facility under the National Collaborative Research Infrastructure Strategy to provide nano and microfabrication facilities for Australia's researchers. This research was also undertaken with the assistance of resources from the National Computational Infrastructure (NCI), which is supported by the Australian Government. A.K. gratefully acknowledges an Australian Research Council Future Fellowship (FT170100373). L.C.H. and F.S. acknowledge funds from the circular economy initiative within the IFM at Deakin University, and thank the ARC (IIC160100032) and Office of Naval Research Global (N62909-18-1-2024) for additional funding. We thank Dr. Jonathan Campbell and Prof. David Lewis for helpful discussions and technical assistance.
Funding Information:
The authors acknowledge financial support from the Australian Research Council (DP200100090), The AMP Tomorrow Fund and the Flinders University Impact Seed Funding for Early Career Researchers (J.M.C.). The authors also acknowledge the support of the Microscopy Australia research facility at Flinders University. This work was performed in part at the South Australian node of the Australian National Fabrication Facility under the National Collaborative Research Infrastructure Strategy to provide nano and microfabrication facilities for Australia's researchers. This research was also undertaken with the assistance of resources from the National Computational Infrastructure (NCI), which is supported by the Australian Government. A.K. gratefully acknowledges an Australian Research Council Future Fellowship (FT170100373). L.C.H. and F.S. acknowledge funds from the circular economy initiative within the IFM at Deakin University, and thank the ARC (IIC160100032) and Office of Naval Research Global (N62909‐18‐1‐2024) for additional funding. We thank Dr. Jonathan Campbell and Prof. David Lewis for helpful discussions and technical assistance.
Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/8/6
Y1 - 2020/8/6
N2 - Inverse vulcanization provides dynamic and responsive materials made from elemental sulfur and unsaturated cross-linkers. These polymers have been used in a variety of applications such as energy storage, infrared optics, repairable materials, environmental remediation, and precision fertilizers. In spite of these advances, there is a need for methods to recycle and reprocess these polymers. In this study, polymers prepared by inverse vulcanization are shown to undergo reactive compression molding. In this process, the reactive interfaces of sulfur polymers are brought into contact by mechanical compression. Upon heating these molds at relatively low temperatures (≈100 °C), chemical bonding occurs at the polymer interfaces by S−S metathesis. This method of processing is distinct from previous studies on inverse vulcanization because the polymers examined in this study do not form a liquid phase when heated. Neither compression nor heating alone was sufficient to mold these polymers into new architectures, so this is a new concept in the manipulation of sulfur polymers. Additionally, high-level ab initio calculations revealed that the weakest S−S bond in organic polysulfides decreases linearly in strength from a sulfur rank of 2 to 4, but then remains constant at about 100 kJ mol−1 for higher sulfur rank. This is critical information in engineering these polymers for S−S metathesis. Guided by this insight, polymer repair, recycling, and repurposing into new composites was demonstrated.
AB - Inverse vulcanization provides dynamic and responsive materials made from elemental sulfur and unsaturated cross-linkers. These polymers have been used in a variety of applications such as energy storage, infrared optics, repairable materials, environmental remediation, and precision fertilizers. In spite of these advances, there is a need for methods to recycle and reprocess these polymers. In this study, polymers prepared by inverse vulcanization are shown to undergo reactive compression molding. In this process, the reactive interfaces of sulfur polymers are brought into contact by mechanical compression. Upon heating these molds at relatively low temperatures (≈100 °C), chemical bonding occurs at the polymer interfaces by S−S metathesis. This method of processing is distinct from previous studies on inverse vulcanization because the polymers examined in this study do not form a liquid phase when heated. Neither compression nor heating alone was sufficient to mold these polymers into new architectures, so this is a new concept in the manipulation of sulfur polymers. Additionally, high-level ab initio calculations revealed that the weakest S−S bond in organic polysulfides decreases linearly in strength from a sulfur rank of 2 to 4, but then remains constant at about 100 kJ mol−1 for higher sulfur rank. This is critical information in engineering these polymers for S−S metathesis. Guided by this insight, polymer repair, recycling, and repurposing into new composites was demonstrated.
KW - composites
KW - inverse vulcanization
KW - recycling
KW - sulfur
KW - sulfur polymer
UR - http://www.scopus.com/inward/record.url?scp=85087044102&partnerID=8YFLogxK
U2 - 10.1002/chem.202001841
DO - 10.1002/chem.202001841
M3 - Article
C2 - 32428387
AN - SCOPUS:85087044102
SN - 1521-3765
VL - 26
SP - 10035
EP - 10044
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 44
ER -