4.7 Article

Co-precipitation synthesis of stable iron oxide nanoparticles with NaOH: New insights and continuous production via flow chemistry

期刊

CHEMICAL ENGINEERING JOURNAL
卷 399, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.125740

关键词

In-situ XRD; In-situ SAXS; Nanoparticle formation kinetics; Co-precipitation; Multistage flow reactor; Continuous production

资金

  1. EPSRC U.K. [EP/M015157/1]
  2. CERIC ERIC internal research project: Nano Analytics in Pharmaceutics
  3. European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant [721290]
  4. FCT [UID/MULTI/04046/2019, PTDC/NAN-MAT/28785/2017]
  5. Fundação para a Ciência e a Tecnologia [PTDC/NAN-MAT/28785/2017] Funding Source: FCT
  6. EPSRC [EP/M015157/1] Funding Source: UKRI

向作者/读者索取更多资源

Co-precipitation is by far the most common synthesis for magnetic iron oxide nanoparticles (IONPs), as cheap and environmentally friendly precursors and simple experimental procedures facilitate IONP production in many labs. Optimising co-precipitation syntheses remains challenging however, as particle formation mechanisms are not well understood. This is partly due to the rapid particle formation (within seconds) providing insufficient time to characterise initial precipitates. To overcome this limitation, a flow chemistry approach has been developed using steady-state operation to freeze transient reaction states locally. This allowed for the first time a comprehensive analysis of the early stages of co-precipitation syntheses via in-situ Small Angle X-ray Scattering and in-situ synchrotron X-Ray Diffraction. These studies revealed that after mixing the ferrous/ferric chloride precursor with the NaOH base solution, the most magnetic iron oxide phase forms within 5 s, the particle size changes only marginally afterwards, and co-precipitation and agglomeration occur simultaneously. As these agglomerates were too large to achieve colloidal stability via subsequent stabiliser addition, co-precipitated IONPs had to be de-agglomerated. This was achieved by adding the appropriate quantity of a citric acid solution which yielded within minutes colloidally stable IONP solutions around a neutral pH value. The new insights into the particle formation and the novel stabilisation procedure (not requiring any ultra-sonication or washing step) allowed to design a multistage flow reactor to synthesise and stabilise IONPs continuously with a residence time of less than 5 min. This reactor was robust against fouling and produced stable IONP solutions (of similar to 1.5 mg particles per ml) reproducibly via fast mixing (< 50 ms) and accurate temperature control at large scale (> 500 ml/h) for low materials cost.

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