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Determination of the Enthalpies of Vaporization of Cyclic Organic Peroxides by Correlation of Changes in Gas Chromatographic Retention Times

机译:通过气相色谱保留时间变化的相关性测定环状有机过氧化物的蒸发焓

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摘要

Liquid and solid cyclic peroxides derived from aliphatic ketones are explosive materials so their enthalpies of vaporization and other thermodynamic or condensed-phase properties cannot be measured directly. In this work the enthalpies of vaporization of peroxides at 298.15 K were estimated simply from gas chromatographic retention times measured at different temperatures. The technique correlates changes in the retention times of compounds whose enthalpies of vaporization are known (called the reference series), with those of the compounds of interest. If t R′ is the adjusted retention time (retention time of each compound minus the retention time of unretained diethyl ether, used as solvent) a plot of ln t R′ against 1/T for each compound (reference compounds and cyclic peroxides) results in a straight line (r 2 > 0.99 for all compounds). The enthalpy of transfer from solution to the vapor state (Δ sol g H m) can be obtained by multiplying the slope by the gas constant (R). A second plot correlates the enthalpies of transfer from solution to the vapor state (Δ sol g H m), as measured by gas–liquid chromatography (GLC), with enthalpies of vaporization of reference materials (Δvap H m at 298.15 K) available in the literature. C9–C15 fatty acid methyl esters and hydrocarbons were used as reference compounds. The enthalpies of vaporization of the cyclic organic peroxides were calculated from the equation of the line obtained in this second correlation, the slope of which was Δvap H m (at 298.15 K)/Δg sol H m. The experiments were performed under isothermal conditions with a DB-5 capillary column, flame-ionization detection (FID), and nitrogen as carrier gas. The column temperature was varied over a range of at least 30–70 K between 403 and 473 K, with chromatograms being acquired at 10 K intervals. Enthalpies of vaporization of cyclic organic peroxides are not available in the literature, and the values given in this paper, obtained by gas chromatography, are the first to be reported.
机译:源自脂肪族酮的液态和固态环状过氧化物是易爆材料,因此无法直接测量其汽化焓和其他热力学或冷凝相性质。在这项工作中,仅通过在不同温度下测量的气相色谱保留时间,即可估算出298.15 K下过氧化物的蒸发焓。该技术将汽化焓已知的化合物(称为参考系列)的保留时间变化与目标化合物的保留时间相关联。如果t R '是调整后的保留时间(每种化合物的保留时间减去未保留的乙醚的保留时间,用作溶剂),则每种化合物的ln t R '对1 / T的图(参考化合物和环状过氧化物)的直线(所有化合物的r 2 g H m )。第二个图将通过气相色谱法(GLC)测量的从溶液转移到气相的焓(Δsol g H m )与文献中提供了参考材料(Δvap H m 在298.15 K)。使用C9 –C15 脂肪酸甲酯和碳氢化合物作为参考化合物。根据在第二次相关中获得的直线方程式,计算环状有机过氧化物的蒸发焓,其斜率为Δvap H m (在298.15 K时)/Δg sol H m 。实验是在等温条件下使用DB-5毛细管柱,火焰电离检测(FID)和氮气作为载气进行的。色谱柱温度在403和473 K之间的至少30–70 K范围内变化,色谱图以10 K的间隔获取。文献中没有提供环状有机过氧化物的汽化焓,而本文首次给出的值是通过气相色谱法获得的。

著录项

  • 来源
    《Chromatographia》 |2007年第2期|31-34|共4页
  • 作者单位

    Laboratorio de Química Facultad de Ingeniería Universidad Nacional del Centro de la Provincia de Buenos Aires Avda. del Valle 5737 B7400JWI Olavarría Buenos Aires Argentina;

    Laboratorio de Química Facultad de Ingeniería Universidad Nacional del Centro de la Provincia de Buenos Aires Avda. del Valle 5737 B7400JWI Olavarría Buenos Aires Argentina;

    Laboratorio de Química Facultad de Ingeniería Universidad Nacional del Centro de la Provincia de Buenos Aires Avda. del Valle 5737 B7400JWI Olavarría Buenos Aires Argentina;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Gas chromatography; Retention data; Enthalpy of vaporization; Organic peroxides;

    机译:气相色谱;保留数据;汽化焓;有机过氧化物;

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