Standard

Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts. / Lee, Chao Wei; Lin, Po Yi; Chen, Bing Hung и др.

в: Catalysis Today, Том 379, 01.11.2021, стр. 124-131.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Lee, CW, Lin, PY, Chen, BH, Kukushkin, RG & Yakovlev, VA 2021, 'Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts', Catalysis Today, Том. 379, стр. 124-131. https://doi.org/10.1016/j.cattod.2020.05.013

APA

Lee, C. W., Lin, P. Y., Chen, B. H., Kukushkin, R. G., & Yakovlev, V. A. (2021). Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts. Catalysis Today, 379, 124-131. https://doi.org/10.1016/j.cattod.2020.05.013

Vancouver

Lee CW, Lin PY, Chen BH, Kukushkin RG, Yakovlev VA. Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts. Catalysis Today. 2021 нояб. 1;379:124-131. Epub 2020 май 11. doi: 10.1016/j.cattod.2020.05.013

Author

Lee, Chao Wei ; Lin, Po Yi ; Chen, Bing Hung и др. / Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts. в: Catalysis Today. 2021 ; Том 379. стр. 124-131.

BibTeX

@article{bc440dc0df8049e2980a52ae7e68f303,
title = "Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts",
abstract = "In this study, Ni and Ni/Mo catalysts supported on zeolite ZSM-5, aka Ni/ZSM-5 and Ni-Mo(R)/ZSM-5, were successfully prepared by the incipient wetness impregnation method to hydrotreat heterogeneously the palmitic acid with an aim for the production of green diesel. Various instruments, such as XRD, SEM, BET, XPS, NH3-TPD and H2-TPR, were employed to characterize these catalysts. The hydrodeoxygenation (HDO) reaction of palmitic acid was carried out in an autoclave at 300 °C with an initial pressure of hydrogen at 35 bar. With Ni-Mo(R)/ZSM-5 catalysts priorly reduced in H2 at 500 °C, the conversion of palmitic acid could reach near 99% after 4 h of HDO reaction at 300 °C. Furthermore, a significant portion of isomerized paraffins appeared in the product, as revealed by GC–MS. That is, both hydrodeoxygenation and hydroisomerization reactions took place conjointly on palmitic acid with Ni-Mo(R)/ZSM-5 catalysts.",
keywords = "Green diesel, Hydrodeoxygenation, Nickel-Molybdenum, Palmitic acid, Zeolite ZSM-5",
author = "Lee, {Chao Wei} and Lin, {Po Yi} and Chen, {Bing Hung} and Kukushkin, {Roman G.} and Yakovlev, {Vadim A.}",
note = "Funding Information: This research is funded by the Ministry of Science and Technology (MoST) of Taiwan and the Russian Science Foundation (RSF) within the framework of the joint grant (RSF Grant No. 18-43-08002 and MOST Grant No. 107-2923-E-006-004-MY3). Funding Information: This research is funded by the Ministry of Science and Technology (MoST) of Taiwan and the Russian Science Foundation (RSF) within the framework of the joint grant (RSF Grant No. 18-43-08002 and MOST Grant No. 107-2923-E-006-004-MY3 ). Publisher Copyright: {\textcopyright} 2020 Elsevier B.V.",
year = "2021",
month = nov,
day = "1",
doi = "10.1016/j.cattod.2020.05.013",
language = "English",
volume = "379",
pages = "124--131",
journal = "Catalysis Today",
issn = "0920-5861",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Hydrodeoxygenation of palmitic acid over zeolite-supported nickel catalysts

AU - Lee, Chao Wei

AU - Lin, Po Yi

AU - Chen, Bing Hung

AU - Kukushkin, Roman G.

AU - Yakovlev, Vadim A.

N1 - Funding Information: This research is funded by the Ministry of Science and Technology (MoST) of Taiwan and the Russian Science Foundation (RSF) within the framework of the joint grant (RSF Grant No. 18-43-08002 and MOST Grant No. 107-2923-E-006-004-MY3). Funding Information: This research is funded by the Ministry of Science and Technology (MoST) of Taiwan and the Russian Science Foundation (RSF) within the framework of the joint grant (RSF Grant No. 18-43-08002 and MOST Grant No. 107-2923-E-006-004-MY3 ). Publisher Copyright: © 2020 Elsevier B.V.

PY - 2021/11/1

Y1 - 2021/11/1

N2 - In this study, Ni and Ni/Mo catalysts supported on zeolite ZSM-5, aka Ni/ZSM-5 and Ni-Mo(R)/ZSM-5, were successfully prepared by the incipient wetness impregnation method to hydrotreat heterogeneously the palmitic acid with an aim for the production of green diesel. Various instruments, such as XRD, SEM, BET, XPS, NH3-TPD and H2-TPR, were employed to characterize these catalysts. The hydrodeoxygenation (HDO) reaction of palmitic acid was carried out in an autoclave at 300 °C with an initial pressure of hydrogen at 35 bar. With Ni-Mo(R)/ZSM-5 catalysts priorly reduced in H2 at 500 °C, the conversion of palmitic acid could reach near 99% after 4 h of HDO reaction at 300 °C. Furthermore, a significant portion of isomerized paraffins appeared in the product, as revealed by GC–MS. That is, both hydrodeoxygenation and hydroisomerization reactions took place conjointly on palmitic acid with Ni-Mo(R)/ZSM-5 catalysts.

AB - In this study, Ni and Ni/Mo catalysts supported on zeolite ZSM-5, aka Ni/ZSM-5 and Ni-Mo(R)/ZSM-5, were successfully prepared by the incipient wetness impregnation method to hydrotreat heterogeneously the palmitic acid with an aim for the production of green diesel. Various instruments, such as XRD, SEM, BET, XPS, NH3-TPD and H2-TPR, were employed to characterize these catalysts. The hydrodeoxygenation (HDO) reaction of palmitic acid was carried out in an autoclave at 300 °C with an initial pressure of hydrogen at 35 bar. With Ni-Mo(R)/ZSM-5 catalysts priorly reduced in H2 at 500 °C, the conversion of palmitic acid could reach near 99% after 4 h of HDO reaction at 300 °C. Furthermore, a significant portion of isomerized paraffins appeared in the product, as revealed by GC–MS. That is, both hydrodeoxygenation and hydroisomerization reactions took place conjointly on palmitic acid with Ni-Mo(R)/ZSM-5 catalysts.

KW - Green diesel

KW - Hydrodeoxygenation

KW - Nickel-Molybdenum

KW - Palmitic acid

KW - Zeolite ZSM-5

UR - http://www.scopus.com/inward/record.url?scp=85084637395&partnerID=8YFLogxK

U2 - 10.1016/j.cattod.2020.05.013

DO - 10.1016/j.cattod.2020.05.013

M3 - Article

AN - SCOPUS:85084637395

VL - 379

SP - 124

EP - 131

JO - Catalysis Today

JF - Catalysis Today

SN - 0920-5861

ER -

ID: 24313877