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Updated: Jan 13, 2026

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Automated closed-loop continuous flow block copolymer synthesizer
Wei Nian Wong1, Daniel J Phillips2, Md Taifur Rahman2
1Polymer Reaction Design Group, School of Chemistry, Monash University 19 Rainforest Walk, Building 23 Clayton VIC 3800 Australia tanja.junkers@monash.edu.
None:
A fully automated continuous flow synthesizer for diblock copolymer (BCP) synthesis was constructed comprising elements of flow chemistry, automation, machine learning and in-line monitoring. A new method using in-line FTIR spectroscopic analysis for accurate determination of monomer conversion (with an error as low as 2% relative to an NMR spectroscopic baseline) is presented, thereby generating a reliable feedback system for reaction self-optimisation using the platform. By employing reversible addition-fragmentation chain transfer (RAFT) polymerization at 100 °C, acrylates and acrylamides of different hydrophilicities (namely methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, ethylene glycol methyl ether acrylate, diethylene glycol ethyl ether acrylate, 2-(dimethylamino)ethyl acrylate, acrylamide & N,N-dimethylacrylamide) were polymerized to make mixed BCPs, targeting different degrees of polymerization (15 to 100). Samples were collected automatically, and a BCP material library comprising 95 diblock copolymers (7 sets of double hydrophobic, 7 sets of amphiphilic and 3 sets of double hydrophilic monomer systems) with M n ranging from 1800 g mol-1 to 14 700 g mol-1, was obtained in a high-throughput manner, with minimal human intervention throughout the entire process.
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