Hydrodealkylation - Revision history

Michel Lamontagne at 18:30, 30 September 2022

2022-09-30T18:30:27Z

Michel Lamontagne at 18:29, 30 September 2022

2022-09-30T18:29:19Z

Michel Lamontagne at 21:07, 10 November 2020

2020-11-10T21:07:06Z

Michel Lamontagne at 21:06, 10 November 2020

2020-11-10T21:06:44Z

Michel Lamontagne: Created page with "'''Hydrodealkylation''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of hydrogen gas t..."

2020-11-04T14:39:27Z

Created page with "'''Hydrodealkylation''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of hydrogen gas t..."

New page

'''[[w:Hydrodealkylation|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of hydrogen gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)

← Older revision		Revision as of 18:30, 30 September 2022
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	'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as [[toluene]], in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)		'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as [[toluene]], in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)

−	It is a process required for [[In-situ resource utilization]]. The main use would be to ~~simplify~~ biological oils created in agriculture into simpler forms for the Martian chemical industry.	+	It is a process required for [[In-situ resource utilization]]. The main use would be to reduce biological oils created in agriculture into simpler forms for the Martian chemical industry.

← Older revision		Revision as of 18:29, 30 September 2022
Line 1:		Line 1:
	'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as [[toluene]], in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)		'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as [[toluene]], in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)

−	It is a process required for [[In-situ resource utilization]].	+	It is a process required for [[In-situ resource utilization]]. The main use would be to simplify biological oils created in agriculture into simpler forms for the Martian chemical industry.

← Older revision		Revision as of 21:07, 10 November 2020
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−	'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)	+	'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as [[toluene]], in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)

	It is a process required for [[In-situ resource utilization]].		It is a process required for [[In-situ resource utilization]].

← Older revision		Revision as of 21:06, 10 November 2020
Line 1:		Line 1:
−	'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of hydrogen gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)	+	'''[[w:Hydrodealkylation\|Hydrodealkylation]]''' is a chemical reaction that often involves reacting an aromatic hydrocarbon, such as toluene, in the presence of [[hydrogen]] gas to form a simpler aromatic hydrocarbon devoid of functional groups. An example is the conversion of 1,2,4-trimethylbenzene to xylene. This chemical process usually occurs at high temperature, at high pressure, or in the presence of a catalyst. These are predominantly transition metals, such as chromium or molybdenum. (ref.:wikipedia)
		+
		+	It is a process required for [[In-situ resource utilization]].