A Raman spectroscopic method for the determination of high pressure vapour liquid equilibria

被引:20
|
作者
Adami, Renata [1 ]
Schuster, Julian [2 ,3 ]
Liparoti, Sara [1 ]
Reverchon, Ernesto [1 ]
Leipertz, Alfred [2 ,3 ]
Braeuer, Andreas [2 ,3 ]
机构
[1] Univ Salerno, Dept Ind Engn, I-84084 Salerno, Italy
[2] Univ Erlangen Nurnberg, Erlangen Grad Sch Adv Opt Technol SAOT, D-91052 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Lehrstuhl Tech Thermodynam, D-91058 Erlangen, Germany
关键词
Vapour liquid equilibria; Raman spectroscopy; In situ measurements; Supercritical CO2; FLUID-PHASE EQUILIBRIA; SUPERCRITICAL ANTISOLVENT PRECIPITATION; CARBON-DIOXIDE; TEMPERATURE-DEPENDENCE; ASSISTED ATOMIZATION; WATER; MIXTURES; ACETONE; SYSTEM; MICROPARTICLES;
D O I
10.1016/j.fluid.2013.09.046
中图分类号
O414.1 [热力学];
学科分类号
摘要
A straight forward and non-invasive strategy to quantify vapour-liquid equilibria (VLE) of the ternary system acetone, water and carbon dioxide (CO2) is reported. The strategy is based on extracting the composition of a ternary mixture from its Raman spectrum. An isolated Raman signal of acetone, which is not interfered with Raman signals of water or CO2, is used as a reference signal. The capability of the strategy introduced is demonstrated by the agreement with VLE data obtained by the other authors that used conventional methods at elevated pressures up to 10 MPa and temperatures up to 353 K. The advantages of the introduced method are its non-invasive sampling method, its insensitivity to misalignment or distortions of the excitation and signal paths as well as power fluctuations of the excitation beam, its fast accessibility to the mixture composition and the general transferability to all systems whose Raman spectrum shows a spectrally isolated strong Raman signal which can be assigned to one specific compound. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:265 / 273
页数:9
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