Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/75602
Title: Preparation of palladium catalysts using the strong electrostatic adsorption technique for stearic acid conversion via the deoxygenation process
Authors: B. Kreatananchai
E. Somsook
T. Kiatsiriroat
K. Punyawudho
Authors: B. Kreatananchai
E. Somsook
T. Kiatsiriroat
K. Punyawudho
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Engineering;Materials Science;Physics and Astronomy
Issue Date: 1-Aug-2021
Abstract: The strong electrostatic adsorption (SEA) technique was used to prepare palladium catalysts on a graphene support to convert stearic acid to diesel-like hydrocarbon via a deoxygenation process. The pH shifts of graphene were determined, and the point of zero charge (PZC) was obtained at pH = 4.6. With a moderately low PZC, the cation Pd precursor (i.e., [Pd(NH3)4]2+—palladium tetraammine—PdTA) was preferred. In the adsorbed conditions, PdTA and the graphene surface attained the strongest electrostatic adsorption at pH = 12 and had the maximum metal surface density around 0.6 μmol/m2. The Pd loading of 5 wt% catalysts was controlled by the initial concentration of PdTA. The Pd particle size distribution was considerably uniform and had a diameter around 2–3 nm according to transmission electron microscopy (TEM). The ring pattern from electron diffraction (ED) and the spectra from X-ray diffraction (XRD) verified that the Pd metal had a face-centered cubic (fcc) crystal structure. The deoxygenation reaction was carried out and reached 99% conversion of stearic acid using 5 wt% Pd/graphene catalysts with mass of 0.6 g. The main product was straight chain hydrocarbon called heptadecane (C17H36), suggesting a decarboxylation pathway. Moreover, the diesel-like hydrocarbon (C16–C21) attained a maximum selectivity at 85.4%.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85111303353&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/75602
ISSN: 21905517
21905509
Appears in Collections:CMUL: Journal Articles

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