Journal
POLYMERS FOR ADVANCED TECHNOLOGIES
Volume 32, Issue 7, Pages 2735-2743Publisher
WILEY
DOI: 10.1002/pat.5220
Keywords
hydrogenation; magnetic nanoparticles; NaOH; palladium; PVP
Categories
Funding
- Committee of Science of the Ministry of Education and Science of the Republic of Kazakhstan [AP05130377]
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Magnetic nanoparticles have gained attention as catalyst supports due to their magnetic separation capability for easy recovery. A proposed synthesis method showed improved activity and lifespan for the Pd magnetic catalyst. The catalyst exhibited high activity and selectivity in phenylacetylene hydrogenation, and could be magnetically recovered and reused multiple times.
Recently, magnetic nanoparticles have attracted the attention as catalyst supports due to the possibility of magnetic separation, allowing for easy, fast, and clean recovery of the catalysts. A synthesis strategy of such supports plays an important role in improving the properties of the magnetic catalysts. Here, we proposed a simple and effective method to increase the activity and lifetime of the Pd magnetic catalyst. Polyvinylpyrrolidone-maghemite nanoparticles were synthesized via one-pot coprecipitation method using an excess of the NaOH. This was followed by adsorption of Pd2+ on the magnetic nanoparticles. The resulting catalyst showed activity (W-C(sic)C = 4.0 x 10(-6) mol s(-1), W-C(sic)C = 12.7 x 10(-6) mol s(-1)) and selectivity (94%) in phenylacetylene hydrogenation. The catalyst was then magnetically recovered and reused 58 times. The activity of the catalyst increased significantly during the first three runs, changing the rate ratio of W-C(sic)C to W-C(sic)C from 1:3.2 to 1:1.6, and then decreased in the following runs. To understand the reason for this behavior, the catalyst was characterized, as well as catalytic studies were performed using similar catalysts for comparison. The results show that the NaOH adsorbed on magnetic support affects the size, stability, and catalytic properties of the Pd particles, and the effect of alkali is enhanced in the presence of the polymer.
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