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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>Semnan University Press</PublisherName>
				<JournalTitle>Journal of Heat and Mass Transfer Research</JournalTitle>
				<Issn>2345-508X</Issn>
				<Volume>9</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2022</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>The Synthesis of Lanthanum Oxide/Ni Catalyst on the CMK-3 for the CO2 reforming of CH4</ArticleTitle>
<VernacularTitle>ساخت کاتالیست اکسید لانتانیوم/ نیکل بر روی مزوپور کربن برای ریفرمینگ گاز متان</VernacularTitle>
			<FirstPage>279</FirstPage>
			<LastPage>288</LastPage>
			<ELocationID EIdType="pii">7731</ELocationID>
			
<ELocationID EIdType="doi">10.22075/jhmtr.2023.25371.1367</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Abass</FirstName>
					<LastName>Kakoo</LastName>
<Affiliation>Facualty of Materials and Metallurgical Engineering, Semnan University, Semnan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mardali</FirstName>
					<LastName>Yousefpor</LastName>
<Affiliation>Facualty of Materials and Metallurgical Engineering, Semnan University, Semnan, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-7240-0877</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2021</Year>
					<Month>11</Month>
					<Day>28</Day>
				</PubDate>
			</History>
		<Abstract>The catalysts with valve metals had been modified to use in the reforming process. Furthermore, there is a trend to the cheaper materials due to the deactivation and high price of the mentioned catalysts. In this case, at the present research work, the Nickel/CMK-3 catalysts with La&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; as the promoter were synthesized by an impregnation method with 3 wt. % of La&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;. Also, the Nickel catalysts/CMK-3 and Nickel catalysts-La&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;/CMK-3 were characterized by N&lt;sub&gt;2&lt;/sub&gt; adsorption-desorption, X-ray diffraction (XRD), Transmission electron microscopy (TEM), Field emission scanning electron microscopy&lt;br /&gt;(FE-SEM), Temperature programmed reduction (TPR), and the performance of the catalysts for CO&lt;sub&gt;2&lt;/sub&gt; reforming of CH&lt;sub&gt;4&lt;/sub&gt;. In addition, the temperature programmed reduction (TPR) technique was selected to evaluate the catalyst properties for the CO&lt;sub&gt;2&lt;/sub&gt; reforming of CH&lt;sub&gt;4&lt;/sub&gt;. In final, the obtained results demonstrated that the formation of amorphous mesoporous Carbon with NiO nanoparticles inside the channels of the supported base and also the Lantana oxide addition induced better Nickel oxide dispersion and increased the interaction of the catalyst particles with support. As a result, the Nickel catalysts supported on the Carbon mesoporous has shown enough activity for the CO&lt;sub&gt;2&lt;/sub&gt; reforming of CH&lt;sub&gt;4&lt;/sub&gt; at 650 &lt;sup&gt;º&lt;/sup&gt;C. However, the mentioned samples were deactivated due to Carbon oxidation according to the TGA results. Therefore, the addition of La&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; with 3 wt. % as a promoter improved the catalytic activity up to 57% and enhanced the catalytic stability at a duration time of 2 hr.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Dioxide carbon gas</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Methane</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">lanthanum oxide</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Promoter</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nickel Catalyst</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://jhmtr.semnan.ac.ir/article_7731_36039e6008d2bab35f89bbf123179c1d.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
