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      <yrYrPub>2006</yrYrPub>
      <sAuthor1>cam</sAuthor1>
      <sAuthor2>flo</sAuthor2>
      <nAuthorn>0</nAuthorn>
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    <eType>journal</eType>
    <eSourceType>Original</eSourceType>
    <sAuthor>Camarillo, E. A.</sAuthor>
    <sAuthor>Flores, H.[Henoc]</sAuthor>
    <sPubName>J. Chem. Thermodyn.</sPubName>
    <yrPubYr>2006</yrPubYr>
    <dateCit>2020-09-29</dateCit>
    <sTitle>Construction, calibration and testing of a micro-combustion calorimeter</sTitle>
    <sAbstract>An isoperibolic micro-combustion calorimeter was designed, built and set up in our laboratory, taking as base a 1107 Parr combustion  bomb of 22 cm3 of volume. Taken into account the geometrical form of the bomb, it was designed and constructed a vessel and a  submarine chamber in brass. All of the pieces of the calorimeter were chromium-plated to reduce heat loss by radiation. The calorimeter  was calibrated by using pellets of standard benzoic acid (mass approximate of 40 mg) leading to the energy equivalent of  e(calor) = (1283.8 +- 0.6) J Ae K 1. In order to test the calorimeter, combustion experiments of salicylic acid were performed leading to  a value of combustion energy of Dcu  =  (21,888.8 +- 10.9) J Ae g 1, which agrees with the reported literature values. The combustion  of piperonylic acid was carried out as a further test leading to a value of combustion energy of Dcu  =  (20,215.9 +- 10.4) J Ae g 1 in accordance  with the reported literature value. The uncertainty of the calibration and the combustion of salicylic acid and piperonylic acid was  0.05%.</sAbstract>
    <sKeyword>Micro-combustion calorimeter</sKeyword>
    <sKeyword>Energy equivalent</sKeyword>
    <sKeyword>Energy of combustion of salicylic acid</sKeyword>
    <sKeyword>Energy of combustion of piperonylic acid</sKeyword>
    <sDOI>10.1016/j.jct.2006.03.001</sDOI>
    <sIDNum>11</sIDNum>
    <sVol>38</sVol>
    <sPage>1269-1273</sPage>
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    </RegNum>
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    <sStandardInChIKey>CURLTUGMZLYLDI-UHFFFAOYSA-N</sStandardInChIKey>
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      <nOrgNum>2</nOrgNum>
    </RegNum>
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    <sStandardInChIKey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</sStandardInChIKey>
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    <RegNum>
      <nOrgNum>3</nOrgNum>
    </RegNum>
    <sStandardInChI>InChI=1S/O2/c1-2</sStandardInChI>
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    <sCommonName>2-hydroxybenzoic acid</sCommonName>
    <sCommonName>benzoic acid, 2-hydroxy-</sCommonName>
    <sCommonName>o-hydroxybenzoic acid</sCommonName>
    <sCommonName>phenol-2-carboxylic acid</sCommonName>
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    <sFormulaMolec>C7H6O3</sFormulaMolec>
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      <eSource>Commercial source</eSource>
      <purity>
        <nStep>1</nStep>
        <ePurifMethod>Crystallization from solution</ePurifMethod>
        <ePurifMethod>Dried by vacuum heating</ePurifMethod>
        <ePurifMethod>Crystallization from solution</ePurifMethod>
        <ePurifMethod>Dried by vacuum heating</ePurifMethod>
      </purity>
      <purity>
        <nStep>2</nStep>
        <nPurityMass>99.8</nPurityMass>
        <nPurityMassDigits>3</nPurityMassDigits>
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    <sStandardInChIKey>VDVJGIYXDVPQLP-UHFFFAOYSA-N</sStandardInChIKey>
    <sCommonName>1,3-benzodioxole-5-carboxylic acid</sCommonName>
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    <sCommonName>benzoic acid, 3,4-(methylenedioxy)-</sCommonName>
    <sCommonName>piperonylic acid</sCommonName>
    <sCommonName>protocatechuic acid methylen ether</sCommonName>
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