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    <identifier>10.57760/sciencedb.j00124.00029</identifier>
    <datestamp>2023-07-28T09:20:47Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2023-07-28</dc:date>
  <dc:title>Catalytic combustion of toluene over cerium modified CuMn/Al2O3/cordierite monolithic catalyst</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00124.00029</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>X-ray diffraction (XRD)&amp;nbsp;patterns&amp;nbsp;from 5 to 85&amp;deg;&amp;nbsp;were performed on Rigaku D/Max 2500&amp;nbsp;instrument equipped with X-ray source of Cu-K&amp;alpha;&amp;nbsp;(&amp;lambda;=1.54056 &amp;Aring;). The N2&amp;nbsp;adsorption-desorption isotherms were obtained at 77 K using Micromeritics 3H-2000PS2. The standard Brunauer-Emmett-Teller (BET)&amp;nbsp;and Barrett-Joyner-Halenda (BJH) methods&amp;nbsp;to calculate the specific surface and pore size, respectively. The morphology and elemental composition of the samples were observed by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX).&amp;nbsp;X-ray photoelectron spectroscopy (XPS) experiments&amp;nbsp;were operated&amp;nbsp;using&amp;nbsp;a ESCALAB 250 with Al K&amp;alpha; (h&amp;nu; = 1486.6 eV) excitation source. The reducibility of sample was characterized by hydrogen temperature-programmed reduction (H2-TPR). Typically,&amp;nbsp;samples&amp;nbsp;(150 mg) were&amp;nbsp;pretreated at 300 &amp;deg;C for 1 h in Ar. The samples were heated from 30 &amp;deg;C to 900 &amp;deg;C in 5% H2/Ar (30 ml/min) at 10 &amp;deg;C/min after cooling to room temperature. For O2-TPD, 100 mg of sample was pretreated under argon at 120 &amp;deg;C&amp;nbsp;for 60 min with a heating ramp of 10&amp;nbsp;&amp;deg;C/min to remove physisorbed gases and residual feed gas. After naturally cooling to room temperature, the gas was switched to 5 vol% O2/Ar and maintained 1 h. Finally, the catalyst was heated with&amp;nbsp;a rate of 10 &amp;deg;C/min&amp;nbsp;from room temperature to 900 &amp;deg;C.&amp;nbsp;&amp;nbsp;In&amp;nbsp;order to evaluate the mechanical stability of the catalyst, the adhesion of the active components of CuMnCex/Al2O3/Cor was tested by ultrasonic vibration method.</dc:description>
  <dc:subject>toluene; catalytic combustion; monolithic catalyst; CuMnCex composite oxide</dc:subject>
  <dc:creator>Dai Yuhang</dc:creator>
  <dc:creator>Li Kaige</dc:creator>
  <dc:creator>Zhao Jinxian</dc:creator>
  <dc:creator>Ren Jun</dc:creator>
  <dc:creator>Quan Yanhong</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.1016/s1872-5813(23)60381-0</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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