Catalytic Methanation of Methanol

Masahiko Matsukata; Tatsuya Hayashi; Masashi Nishiyama; Eiichi Kikuchi; Yoshiro Morita

doi:10.1627/jpi1958.30.265

Catalytic Methanation of Methanol

Masahiko Matsukata, Tatsuya Hayashi, Masashi Nishiyama, Eiichi Kikuchi, Yoshiro Morita

School of Advanced Science and Engineering

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

Abstract

To produce town gas catalytic methanation of methanol was investigated in the temperature range of 300—350°C. Nickel and alumina were excellent components of the catalyst. The catalysts containing 80wt% of nickel prepared by coprecipitation methods showed especially high activities at 300°C. The methanol conversion over the coprecipitated catalysts was dependent upon the size of the nickel crystallite, while the methane selectivities were not. The activity and selectivity of coprecipitated catalysts were steady during a 20hr-run and on addition of water to methanol.

Original language	English
Pages (from-to)	265-272
Number of pages	8
Journal	Journal of The Japan Petroleum Institute
Volume	30
Issue number	4
DOIs	https://doi.org/10.1627/jpi1958.30.265
Publication status	Published - 1987

Keywords

Catalyst preparation
Coprecipitation method
Metal catalyst
Methane
Methanol
Reaction mechanism

ASJC Scopus subject areas

Fuel Technology
Energy Engineering and Power Technology

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title = "Catalytic Methanation of Methanol",

abstract = "To produce town gas catalytic methanation of methanol was investigated in the temperature range of 300—350°C. Nickel and alumina were excellent components of the catalyst. The catalysts containing 80wt% of nickel prepared by coprecipitation methods showed especially high activities at 300°C. The methanol conversion over the coprecipitated catalysts was dependent upon the size of the nickel crystallite, while the methane selectivities were not. The activity and selectivity of coprecipitated catalysts were steady during a 20hr-run and on addition of water to methanol.",

keywords = "Catalyst preparation, Coprecipitation method, Metal catalyst, Methane, Methanol, Reaction mechanism",

author = "Masahiko Matsukata and Tatsuya Hayashi and Masashi Nishiyama and Eiichi Kikuchi and Yoshiro Morita",

year = "1987",

doi = "10.1627/jpi1958.30.265",

language = "English",

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T1 - Catalytic Methanation of Methanol

AU - Matsukata, Masahiko

AU - Hayashi, Tatsuya

AU - Nishiyama, Masashi

AU - Kikuchi, Eiichi

AU - Morita, Yoshiro

PY - 1987

Y1 - 1987

N2 - To produce town gas catalytic methanation of methanol was investigated in the temperature range of 300—350°C. Nickel and alumina were excellent components of the catalyst. The catalysts containing 80wt% of nickel prepared by coprecipitation methods showed especially high activities at 300°C. The methanol conversion over the coprecipitated catalysts was dependent upon the size of the nickel crystallite, while the methane selectivities were not. The activity and selectivity of coprecipitated catalysts were steady during a 20hr-run and on addition of water to methanol.

AB - To produce town gas catalytic methanation of methanol was investigated in the temperature range of 300—350°C. Nickel and alumina were excellent components of the catalyst. The catalysts containing 80wt% of nickel prepared by coprecipitation methods showed especially high activities at 300°C. The methanol conversion over the coprecipitated catalysts was dependent upon the size of the nickel crystallite, while the methane selectivities were not. The activity and selectivity of coprecipitated catalysts were steady during a 20hr-run and on addition of water to methanol.

KW - Catalyst preparation

KW - Coprecipitation method

KW - Metal catalyst

KW - Methane

KW - Methanol

KW - Reaction mechanism

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DO - 10.1627/jpi1958.30.265

M3 - Article

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EP - 272

JO - Sekiyu Gakkaishi (Journal of the Japan Petroleum Institute)

JF - Sekiyu Gakkaishi (Journal of the Japan Petroleum Institute)

SN - 1346-8804

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ER -

Catalytic Methanation of Methanol

Abstract

Keywords

ASJC Scopus subject areas

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