Synthesis of Filamentary Carbon Material on a Self-Organizing Ni–Pt Catalyst in the Course of 1,2-Dichloroethane Decomposition
- Authors: Bauman Y.I.1, Rudneva Y.V.2, Mishakov I.V.1,3, Plyusnin P.E.2,4, Shubin Y.V.2,4, Vedyagin A.A.1,3
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Affiliations:
- Boreskov Institute of Catalysis, Siberian Branch
- Nikolaev Institute of Inorganic Chemistry, Siberian Branch
- National Research Tomsk Polytechnic University
- Novosibirsk State University
- Issue: Vol 59, No 3 (2018)
- Pages: 363-371
- Section: Article
- URL: https://journal-vniispk.ru/0023-1584/article/view/163840
- DOI: https://doi.org/10.1134/S0023158418030023
- ID: 163840
Cite item
Abstract
A series of model microdisperse Ni1–xPtx alloys (x =0–0.05) was synthesized by a coprecipitation method with the subsequent sintering of the precipitate in an atmosphere of H2 at 800°C. Their chemical and phase compositions were determined (by AAS and XRD analysis, respectively), and it was found that the synthesis method proposed afforded Ni–Pt solid solutions based on the face-centered nickel lattice. The kinetic features of the carbon erosion of Ni1–xPtx alloys in their contact with 1,2-dichloroethane vapor in a temperature range of 550–700°C were studied. It was found that the presence of Pt in the alloy increased the rate of accumulation of carbon product by a factor of ~1.5 regardless of the concentration of Pt. The catalyst did not undergo deactivation for 5 h of reaction to ensure a high yield of carbon material (103 g/gCat). With the use of electron microscopy (SEM and TEM techniques), it was found that the carbon product consisted of carbon fibers with a segmented structure. An increase in the concentration of Pt in the alloy to 4.3 wt % sharply changed the disintegration of the alloy to cause the formation of carbon product with a bimodal fiber diameter distribution (dav = 0.4 and 1.2 μm).
About the authors
Yu. I. Bauman
Boreskov Institute of Catalysis, Siberian Branch
Author for correspondence.
Email: bauman@catalysis.ru
Russian Federation, Novosibirsk, 630090
Yu. V. Rudneva
Nikolaev Institute of Inorganic Chemistry, Siberian Branch
Email: bauman@catalysis.ru
Russian Federation, Novosibirsk, 630090
I. V. Mishakov
Boreskov Institute of Catalysis, Siberian Branch; National Research Tomsk Polytechnic University
Email: bauman@catalysis.ru
Russian Federation, Novosibirsk, 630090; Tomsk, 634050
P. E. Plyusnin
Nikolaev Institute of Inorganic Chemistry, Siberian Branch; Novosibirsk State University
Email: bauman@catalysis.ru
Russian Federation, Novosibirsk, 630090; Novosibirsk, 630090
Yu. V. Shubin
Nikolaev Institute of Inorganic Chemistry, Siberian Branch; Novosibirsk State University
Email: bauman@catalysis.ru
Russian Federation, Novosibirsk, 630090; Novosibirsk, 630090
A. A. Vedyagin
Boreskov Institute of Catalysis, Siberian Branch; National Research Tomsk Polytechnic University
Email: bauman@catalysis.ru
Russian Federation, Novosibirsk, 630090; Tomsk, 634050
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