Abstract

Despite the wide usage of magnetic nanoparticles, it remains challenging to synthesise particles with properties that exploit each application's full potential. Time consuming experimental procedures and particle analysis hinder process development, which is commonly constrained to a handful of experiments without considering particle formation kinetics, reproducibility and scalability. Flow reactors are known for their potential of large-scale production and high-throughput screening of process parameters. These advantages, however, have not been utilised for magnetic nanoparticle synthesis where particle characterisation is performed, with a few exceptions, post-synthesis. To overcome this bottleneck, we developed a highly sensitive magnetometer for flow reactors to characterise magnetic nanoparticles in solution in-line and in real-time using alternating current susceptometry. This flow magnetometer enriches the flow-chemistry toolbox by facilitating continuous quality control and high-throughput screening of magnetic nanoparticle syntheses. The sensitivity required to monitor magnetic nanoparticle syntheses at the typically low concentrations (<100 mM of Fe) was achieved by comparing the signals induced in the sample and reference cell, each of which contained near-identical pairs of induction and pick-up coils. The reference cell was filled only with air, whereas the sample cell was a flow cell allowing sample solution to pass through. Balancing the flow and reference cell impedance with a newly developed electronic circuit was pivotal for the magnetometer's sensitivity. To showcase its potential, the flow magnetometer was used to monitor two iron oxide nanoparticle syntheses with well-known particle formation kinetics, i.e., co-precipitation syntheses with sodium carbonate and sodium hydroxide as base, which have been previously studied via synchrotron X-ray diffraction. The flow magnetometer facilitated batch (on-line) and flow (in-line) synthesis monitoring, providing new insights into the particle formation kinetics as well as, effect of temperature and pH. The compact lab-scale flow device presented here, opens up new possibilities for magnetic nanoparticle synthesis and manufacturing, including 1) early stage reaction characterisation 2) process monitoring and control and 3) high-throughput screening in combination with flow reactors.

Highlights

  • Magnetic nanoparticles (MNPs) containing iron, cobalt or nickel, form a class of materials whose properties are of great interest to the fields of electronics, separation and purification, catalysis, and especially biomedicine.[1,2,3,4,5,6] The applications utilising MNPs have in common the need for distinct particle characteristics in terms of size, magnetic moment, surface chemistry, colloidal stability, etc

  • The X-ray diffraction (XRD) analysis confirmed the results obtained via the in-line magnetometer that is: i) the presence of magnetite; ii) the sensitivity of the onset of magnetite formation to the temperature in the range of 30–45 °C (Fig. S8† shows the iron oxide nano particles (IONPs) solutions beside a magnet); and revealed that the final MNP size does not correlate with the period of time required for the transition to magnetite

  • For the IONP co-precipitation synthesis using sodium hydroxide, we have shown in previous work that magnetite forms rapidly.[27,41]

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Summary

Introduction

Magnetic nanoparticles (MNPs) containing iron, cobalt or nickel, form a class of materials whose properties are of great interest to the fields of electronics, separation and purification, catalysis, and especially biomedicine.[1,2,3,4,5,6] The applications utilising MNPs have in common the need for distinct particle characteristics in terms of size, magnetic moment, surface chemistry, colloidal stability, etc. The flow magnetometer was used to monitor several IONP co-precipitation syntheses of which insights into the particle formation are available from in situ XRD and SAXS analysis.[23,27] Our inexpensive, compact and easy to use device confirmed known kinetics and provided new information on the temperature and pH dependence of the magnetic iron oxide phase formation.

Results
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