On-line and real-time monitoring of organophilic pervaporation by mass spectrometry

被引:10
|
作者
Brazinha, Carla [1 ]
Fonseca, A. P. [2 ]
Teodoro, O. M. N. D. [2 ]
Crespo, Joao G. [1 ]
机构
[1] Univ Nova Lisboa, FCT, Dept Chem, REQUIMTE CQFB, P-2829516 Caparica, Portugal
[2] Univ Nova Lisboa, FCT, Dept Phys, CEFITEC, P-2829 Caparica, Portugal
关键词
Organophilic pervaporation; Fractionated condensation; Aroma/flavour recovery; Bioethanol; On-line mass spectrometry; Real-time monitoring; AROMA COMPOUNDS; SEPARATION; RECOVERY; MIXTURES; SORPTION;
D O I
10.1016/j.memsci.2009.10.009
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This work demonstrates experimentally the use of mass spectrometry (MS) for on-line, quantitative monitoring of organophilic pervaporation processes operated not only under variable conditions of temperature of condensation/downstream pressure but also when using complex multi-component feed streams. Due to its high sensitivity, mass spectrometry is particularly suitable for on-line monitoring of aromas in dilute streams under reduced pressure, as happens with natural aromas in permeate streams. Mass spectrometry is also suitable for on-line monitoring of solvent and co-solvent permeants (water and ethanol in the selected case study), enabling for on-line determination of selectivity of the solutes of interest. A new method of calibration is proposed and validated, which correlates the intensity of the characteristic mass peak m(i)/z for each compound of interest with its partial pressure in the permeate stream. Moreover, mass spectrometry proves to be a powerful tool for studying the fractionation of aromas, recovered by integrated pervaporation-condensation processes, allowing on-line monitoring of each solute vapour in the permeate stream. Additionally, this technique enables for accurate transient studies due to the possibility of acquiring one data point every 12-15 s (potentially less, if desired) in real-time. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 92
页数:10
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