Abstract

Hybrid gel beads based on combining a low‐molecular‐weight gelator (LMWG) with a polymer gelator (PG) demonstrate an enhanced ability to self‐propel in water, with the LMWG playing an active role. Hybrid gel beads were loaded with ethanol and shown to move in water owing to the Marangoni effect changes in surface tension caused by the expulsion of ethanol – smaller beads move farther and faster than larger beads. Flat shapes of the hybrid gel were cut using a “stamp” – circles moved the furthest, whereas stars showed more rotation on their own axes. Comparing hybrid LMWG/PG gel beads with PG‐only beads demonstrated that the LMWG speeds up the beads, enhancing the rate of self‐propulsion. Self‐assembly of the LMWG into a “solid‐like” network prevents its leaching from the gel. The LMWG also retains its own unique function – specifically, remediating methylene blue pollutant dye from basic water as a result of noncovalent interactions. The mobile hybrid beads accumulate this dye more effectively than PG‐only beads. Self‐propelling gel beads have potential applications in removal/delivery of active agents in environmental or biological settings. The ability of self‐assembling LMWGs to enhance mobility and control removal/delivery suggests that adding them to self‐propelling systems can add significant value.

Highlights

  • Self-assembled hydrogels are fascinating responsive soft materials with potential applications ranging from environmental regeneration to tissue engineering.[1]

  • It has recently been demonstrated that combining low-molecularweight gelator (LMWG) with the polymer gelator (PG) calcium alginate can give rise to well-defined gel beads of sizes ranging from several millimeters to 800 nm.[5]

  • DBS-CONHNH2/agarose two-component gel beads were obtained by an emulsion method, using a 0.3% wt/vol concentration of the LMWG and a 1.0% wt/vol concentration of the PG

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Summary

Introduction

Self-assembled hydrogels are fascinating responsive soft materials with potential applications ranging from environmental regeneration to tissue engineering.[1]. The data indicate that the gel bead diameter significantly influences the total distance travelled and their average speed in the first 5 and 30 seconds (Figure S12-S14, Table S4).

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