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  1. 学術雑誌論文
  2. 5 技術(工学)

The role of Ce addition in catalytic activity enhancement of TiO2-supported Ni for CO2 methanation reaction

http://hdl.handle.net/10228/00008007
http://hdl.handle.net/10228/00008007
fd127a1a-7874-4519-aef3-4901c3b841a7
名前 / ファイル ライセンス アクション
d0ra04934d.pdf d0ra04934d.pdf (2.9 MB)
アイテムタイプ 学術雑誌論文 = Journal Article(1)
公開日 2021-01-12
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
タイトル
タイトル The role of Ce addition in catalytic activity enhancement of TiO2-supported Ni for CO2 methanation reaction
言語 en
言語
言語 eng
著者 Makdee, Ammarika

× Makdee, Ammarika

WEKO 28813

en Makdee, Ammarika
Makdee, A.

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Chanapattharapol, Kingkaew Chayakul

× Chanapattharapol, Kingkaew Chayakul

WEKO 28814

en Chanapattharapol, Kingkaew Chayakul
Chanapattharapol, K.C.

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Kidkhunthod, Pinit

× Kidkhunthod, Pinit

WEKO 28815

en Kidkhunthod, Pinit
Kidkhunthod, P.

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Poo-arporn, Yingyot

× Poo-arporn, Yingyot

WEKO 28816

en Poo-arporn, Yingyot
Poo-Arporn, Y.

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横野, 照尚

× 横野, 照尚

WEKO 6794
e-Rad 10203887
Scopus著者ID 7402659316
ORCiD 0000-0002-7825-8189

ja 横野, 照尚

en Ohno, Teruhisa

ja-Kana オウノ, テルヒサ


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抄録
内容記述タイプ Abstract
内容記述 In this work, various amounts of Ce were added to TiO2 to form a mixed oxide support; CexTi1−xO2 (x = 0, 0.003, 0.05, 0.10 and 0.15) and then those synthesized supports were impregnated by 10 wt% Ni to produce a catalysts. The 10 wt% Ni–CexTi1−xO2 (x = 0, 0.003, 0.05, 0.10 and 0.15) catalysts were tested for CO2 methanation reaction by using a fixed-bed reactor in the temperature range of 100–500 °C. The sample was pretreated at 450 °C under H2 and then a mixed feed gas of CO2 and H2 was switched into the reactor to start the reaction. The results showed that 10 wt% Ni–Ce0.003Ti0.997O2 catalyst (the lowest Ce content) exhibited the highest CO2 conversion and CH4 yield. Moreover, 10 wt% Ni–Ce0.003Ti0.997O2 showed highly stable during the stability test (50 h.). The results indicated that upon addition of small amount of Ce into TiO2-supported Ni, the surface, structural, electrical and redox properties of the catalyst were improved to the extent that these properties can promote the catalytic activities for CO2 methanation. The Ce addition can improve the CO2 methanation catalytic activity by several ways. First, higher dispersion of Ni on catalysts surface upon addition of Ce was observed which resulted in higher adsorption rate of H2 on this metal active site. Second, formation of a larger amounts of oxygen vacancies as well as basicity improvement upon addition of Ce were occurred which can increase the CO2 adsorption on catalyst surface. Third, incorporation of Ce resulted in improving of a starting reduction temperature of Ni2+ to Ni0 for TiO2-supported Ni catalyst which can indicate that the reducibility of Ce-doped TiO2-supported Ni catalyst was enhanced and then alter its catalytic activity. However, increasing of Ce content led to lowering of CO2 methanation activities which resulted from increasing of basicity by Ce addition. The excess amounts of adsorbed CO2 would lead to competitive adsorption to H2 and then lead to a decrease of catalytic activity. Therefore, an appropriate amount of H2 and CO2 adsorption ability on catalyst surface was a prominent factor to dominate the catalytic activity.
言語 en
書誌情報 en : RSC Advances

巻 10, 号 45, p. 26952-26971, 発行日 2020-07-20
出版社
出版者 Royal Society of Chemistry
言語 en
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.1039/D0RA04934D
日本十進分類法
主題Scheme NDC
主題 572
ISSN
収録物識別子タイプ EISSN
収録物識別子 2046-2069
著作権関連情報
権利情報 Copyright (c) The Royal Society of Chemistry 2020 This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
査読の有無
値 yes
研究者情報
URL https://hyokadb02.jimu.kyutech.ac.jp/html/98_ja.html
論文ID(連携)
値 10360480
連携ID
値 8527
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