首页> 外文OA文献 >I. Latent heat of vaporization of n-hexane; II. Volumetric and latent heat of vaporization measurements for trans-2-butene; III. Partial enthalpy change upon vaporization for n-butane in the n-butane-n-decane system
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I. Latent heat of vaporization of n-hexane; II. Volumetric and latent heat of vaporization measurements for trans-2-butene; III. Partial enthalpy change upon vaporization for n-butane in the n-butane-n-decane system

机译:I.正己烷蒸发潜热; II。反式-2-丁烯的蒸发量的体积和潜热; III。在正丁烷-n-癸烷体系中正丁烷蒸发时的部分焓变化

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摘要

NOTE: Text or symbols not renderable in plain ASCII are indicated by [...]. Abstract is included in .pdf document. ududI. The enthalpy change upon vaporization of n-hexane was experimentally determined by calorimetric measurements at temperatures between 100[degrees] and 340[degrees]F. The results are presented in tabular and graphical form. Good agreement is indicated with the limited data available.ududII. The specific volumes of the liquid and dense phase of trans-2-butene were measured at pressures up to 5000 pounds per square inch in the temperature interval between 40[degrees] and 400[degrees]F. The latent heat of vaporization was determined from calorimetric measurements at temperatures between 100[degrees] and 250[degrees]F. The results are presented in graphical and tabular form together with comparisons with earlier published data.ududIII. The enthalpy change upon vaporization, often referred to as the differential latent heat of vaporization, has been measured for the n-butane-n-decane system by calorimetric techniques. The measurements covered the complete composition range in the temperature interval between 100[degrees] and 340[degrees]F. The partial enthalpy change upon vaporization for n-butane was determined by applying a correction for the presence of small amounts of n-decane in the vapor. The partial internal energy change upon vaporization for n-butane was also computed. The results are presented in graphical and tabular form. A general thermodynamic analysis for withdrawal or addition of material to an isochoric vessel containing coexisting phases of a multi-component system is presented
机译:注意:用[...]表示无法用纯ASCII呈现的文本或符号。摘要包含在.pdf文件中。 ud udI。通过在100°F和340°F之间的温度通过量热法测量,实验确定了正己烷蒸发后的焓变。结果以表格和图形形式显示。 ud udII。表示可用有限的数据达成良好的一致性。反式-2-丁烯的液相和致密相的比容是在40°F至400°F的温度区间内,在高达每平方英寸5000磅的压力下测量的。汽化潜热是根据量热法在100°F至250°F之间的温度确定的。结果以图形和表格形式显示,并与以前发布的数据进行比较。 ud udIII。已经通过量热技术测量了正丁烷-正癸烷体系的汽化焓变化(通常称为汽化潜热差)。测量覆盖了100°F至340°F温度范围内的整个成分范围。通过对蒸气中少量正癸烷的存在进行校正,可以确定正丁烷蒸发时的部分焓变化。还计算了正丁烷汽化时的部分内部能量变化。结果以图形和表格形式显示。提出了将物料抽出或添加到包含多组分系统共存相的等容容器中的常规热力学分析

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    Huisman Johannes;

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  • 年度 1964
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