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  <titleInfo>
    <title>Nickel-cerium bimetallic catalyst on zeolite naa derived from kaolin for carbon dioxide methanation</title>
  </titleInfo>
  <name type="personal">
    <namePart>Raja Nurain Nabilah Binti Raja Alias</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
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  <typeOfResource manuscript="yes">text</typeOfResource>
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    <place>
      <placeTerm type="code" authority="marccountry">my</placeTerm>
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    <dateIssued encoding="marc">2025</dateIssued>
    <copyrightDate encoding="marc">2025</copyrightDate>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
    <extent>xii , 87 pages : illustrations ;</extent>
  </physicalDescription>
  <abstract>CO2 is a colorless, non-flammable gas at normal temperatures and pressures. Its excessive  buildup in the atmosphere absorbs solar radiation, resulting in a greenhouse effect that causes  global warming and rising temperatures. Stabilizing CO2 levels is crucial for reducing climate  change. Catalytic conversion is a potential strategy for converting CO2 into usable industrial  products like methane. This work developed a Ni/Ce/Ru catalyst based on NaA zeolite,  manufactured from natural kaolin, for CO2 methanation. The hydrothermally produced NaA  zeolite had a large surface area and was thermally stable, making it an efficient support  material. The catalyst, synthesized via the wet impregnation method using kaolin-derived  zeolite NaA, exhibited excellent CO2 methanation performance under mild conditions (200– 350ºC), achieving a maximum CO2 conversion of 82.6% at 350ºC and CH4 selectivity  exceeding 90%. The optimal composition, 90Ni/10Ce/1Ru, demonstrated the synergistic role  of Ce as a co-dopant and Ru as a promoter, as validated by gas chromatography. Structural  characterization via Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction  (XRD), Brunauer-Emmett-Teller (BET), and Scanning Electron Microscopy (SEM) confirmed  the catalyst’s enhanced properties, including active NiO (37.40º, 43.37º, 62.90º, 75.60º, 79.43º)  and CeO2 (28.62º, 33.15º, 47.56º) phases, improved metal-support interactions, and thermal  stability. The Ru addition caused a reduction in BET surface area (7.3656 m2 /g to 5.5960 m2 /g),  pore volume (0.024540 cm3 /g to 0.024345 cm3 /g), and average pore diameter (10.275 Å to  9.730 Å), indicating structural modifications. SEM analysis further revealed a well-dispersed  nanoscale morphology that prevents sintering and enhances catalytic activity. This study  demonstrates the feasibility of using locally plentiful kaolin as a sustainable and cost-effective  material for catalytic applications. By successfully decreasing greenhouse gas emissions and  promoting renewable energy programs, the created catalyst helps to long-term solutions to  global climate concerns.</abstract>
  <targetAudience authority="marctarget">specialized</targetAudience>
  <note type="statement of responsibility">Raja Nurain Nabilah Binti Raja Alias</note>
  <note>Faculty of Industrial Sciences and Technology</note>
  <note>Final Year Report (Bachelor of Applied Science of Industrial Chemistry) -- Universiti Malaysia Pahang Al-Sultan Abdullah - 2025</note>
  <note>Include bibliographical reference</note>
  <subject authority="lcsh">
    <name type="corporate">
      <namePart>Faculty of Industrial Sciences and Technology</namePart>
    </name>
    <topic>Dissertations</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Universities and colleges</topic>
    <topic>Dissertations</topic>
  </subject>
  <identifier type="isbn">THE0010506 (Local)</identifier>
  <identifier type="uri">https://umpir.ump.edu.my/id/eprint/46187</identifier>
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    <url>https://umpir.ump.edu.my/id/eprint/46187</url>
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    <recordCreationDate encoding="marc">260427</recordCreationDate>
    <recordChangeDate encoding="iso8601">20260427143641.0</recordChangeDate>
    <languageOfCataloging>
      <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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