Synthesis of Tailored Segmented Polyurethanes Utilizing Continuous-Flow Reactors and Real-Time Process MonitoringClick to copy article linkArticle link copied!
- Xabier Lopez de ParizaXabier Lopez de ParizaIBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesPOLYMAT, University of the Basque Country UPV/EHU, Joxe Mari Korta Center, Avda. Tolosa 72, Donostia-San Sebastian 20018, SpainMore by Xabier Lopez de Pariza
- Tim Erdmann*Tim Erdmann*Email: [email protected]IBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesMore by Tim Erdmann
- Pedro L. ArrecheaPedro L. ArrecheaIBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesMore by Pedro L. Arrechea
- Leron PerezLeron PerezIBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesMore by Leron Perez
- Charles DausseCharles DausseIBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesMore by Charles Dausse
- Nathaniel H. ParkNathaniel H. ParkIBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesMore by Nathaniel H. Park
- James L. HedrickJames L. HedrickIBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United StatesMore by James L. Hedrick
- Haritz Sardon*Haritz Sardon*Email: [email protected]POLYMAT, University of the Basque Country UPV/EHU, Joxe Mari Korta Center, Avda. Tolosa 72, Donostia-San Sebastian 20018, SpainMore by Haritz Sardon
Abstract

Conducting polymerizations under continuous-flow conditions affords distinct advantages over batch experimentation and has increasingly been employed by the research community for chain-growth polymerizations to accelerate material discovery and to finely tune material properties. This work now expands on the reported advances by demonstrating the utility of continuous flow for polyaddition reactions of polyurethanes (PUs). Various reactor configurations enable the on-demand organocatalytic one-step synthesis of linear PUs with tailored soft-to-hard segment ratios in 3–5 min at room temperature. In-line analytics is implemented for real-time process monitoring and to develop process control mechanisms, increasing the control over monomer conversion and material quality and minimizing batch-to-batch variations. The reported strategies thus provide a guideline for the straightforward preparation of libraries of commercially relevant PU materials.
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