Synthesis of Ni nanoparticles with controllable magnetic properties by atmospheric pressure microplasma assisted process

22Citations
Citations of this article
49Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

An atmospheric pressure microplasma technique is demonstrated for the gas phase synthesis of Ni nanoparticles by plasma-assisted nickelocene dissociation at different conditions. The dissociation process and the products are characterized by complementary analytical methods to establish the relationship between operational conditions and product properties. The innovation is to show proof-of-principle of a new synthesis route which offers access to less costly and less poisonous reactant, a higher quality product, and a simple, continuous and pre/post treatment-free manner with chance for fine-tuning “in-flight.” Results show that Ni nanoparticles with controllable magnetic properties are obtained, in which flexible adjustment of product properties can be achieved by tuning operational parameters. At the optimized condition only fcc Ni nanoparticles are formed, with saturation magnetization value of 44.4 mAm2/g. The upper limit of production rate for Ni nanoparticles is calculated as 4.65 × 10−3 g/h using a single plasma jet, but the process can be scaled-up through a microplasma array design. In addition, possible mechanisms for plasma-assisted nickelocene dissociation process are discussed. © 2017 The Authors AIChE Journal published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers AIChE J, 64: 1540–1549, 2018.

Cite

CITATION STYLE

APA

Lin, L., Li, S., Hessel, V., Starostin, S. A., Lavrijsen, R., & Zhang, W. (2018). Synthesis of Ni nanoparticles with controllable magnetic properties by atmospheric pressure microplasma assisted process. AIChE Journal, 64(5), 1540–1549. https://doi.org/10.1002/aic.16054

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free