ThermoML Data file

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Information on ThermoML


<?xml version="1.0" encoding="UTF-8"?> <!--Created by Guided Data Capture (GDC) Software (http://www.trc.nist.gov)--> <DataReport xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:noNamespaceSchemaLocation="http://www.trc.nist.gov/ThermoML.xsd"> <Version> <nVersionMajor>2</nVersionMajor> <nVersionMinor>0</nVersionMinor> </Version> <Citation> <TRCRefID> <yrYrPub>2006</yrYrPub> <sAuthor1>ozm</sAuthor1> <sAuthor2/> <nAuthorn>0</nAuthorn> </TRCRefID> <eType>journal</eType> <eSourceType>Original</eSourceType> <sAuthor>Ozmen, D.[Dilek]</sAuthor> <sPubName>Fluid Phase Equilib.</sPubName> <yrPubYr>2006</yrPubYr> <dateCit>2006-12-14</dateCit> <sTitle>(Liquid + liquid) equilibria of (water + propionic acid + methyl isoamyl ketone or diisobutyl ketone or ethyl isoamyl keton) at T = 298.2 K</sTitle> <sKeyword>LLE</sKeyword> <sKeyword>Propionic acid</sKeyword> <sKeyword>Methyl isoamyl ketone</sKeyword> <sKeyword>Diisobutyl ketone</sKeyword> <sKeyword>Ethyl isoamyl ketone</sKeyword> <sVol>250</sVol> <sPage>70-75</sPage> </Citation> <Compound> <RegNum> <nOrgNum>1</nOrgNum> </RegNum> <sCommonName>water</sCommonName> <sFormulaMolec>H2O</sFormulaMolec> <Sample> <nSampleNm>1</nSampleNm> <eSource>Synthesized by the authors</eSource> <purity> <nStep>1</nStep> <ePurifMethod>Fractional distillation</ePurifMethod> </purity> <purity> <nStep>1</nStep> <nUnknownPerCent>99.5</nUnknownPerCent> <nUnknownPerCentDigits>3</nUnknownPerCentDigits> <eAnalMeth>Estimated by the compiler</eAnalMeth> </purity> </Sample> </Compound> <Compound> <RegNum> <nOrgNum>2</nOrgNum> </RegNum> <sCommonName>propanoic acid</sCommonName> <sFormulaMolec>C3H6O2</sFormulaMolec> <Sample> <nSampleNm>1</nSampleNm> <eSource>Commercial source</eSource> <purity> <nStep>1</nStep> <nPurityMass>99</nPurityMass> <nPurityMassDigits>2</nPurityMassDigits> <eAnalMeth>Stated by supplier</eAnalMeth> </purity> </Sample> </Compound> <Compound> <RegNum> <nOrgNum>3</nOrgNum> </RegNum> <sCommonName>5-methyl-2-hexanone</sCommonName> <sFormulaMolec>C7H14O</sFormulaMolec> <Sample> <nSampleNm>1</nSampleNm> <eSource>Commercial source</eSource> <purity> <nStep>1</nStep> <nPurityMass>99</nPurityMass> <nPurityMassDigits>2</nPurityMassDigits> <eAnalMeth>Stated by supplier</eAnalMeth> </purity> </Sample> </Compound> <Compound> <RegNum> <nOrgNum>4</nOrgNum> </RegNum> <sCommonName>2,6-dimethyl-4-heptanone</sCommonName> <sFormulaMolec>C9H18O</sFormulaMolec> <Sample> <nSampleNm>1</nSampleNm> <eSource>Commercial source</eSource> <purity> <nStep>1</nStep> <nPurityMass>99</nPurityMass> <nPurityMassDigits>2</nPurityMassDigits> <eAnalMeth>Stated by supplier</eAnalMeth> </purity> </Sample> </Compound> <Compound> <RegNum> <nOrgNum>5</nOrgNum> </RegNum> <sCommonName>3-heptanone, 6-methyl-</sCommonName> <sFormulaMolec>C8H16O</sFormulaMolec> <Sample> <nSampleNm>1</nSampleNm> <eSource>Commercial source</eSource> <purity> <nStep>1</nStep> <nPurityMass>99</nPurityMass> 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