http://www.cnr.it/ontology/cnr/individuo/prodotto/ID55038
Comparative study of sorption and permeation techniques for the determination of heptane and toluene transport in polyethylene membranes (Articolo in rivista)
- Type
- Label
- Comparative study of sorption and permeation techniques for the determination of heptane and toluene transport in polyethylene membranes (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.memsci.2009.04.030 (literal)
- Alternative label
Friess,K., Jansen, J.C., Vopicka, O., Randová, A., Hynek, V., Sípek, M., Bartovská, L., Izák, P., Dingemans, m., Dewulf, J., Van Langenhove, H., Drioli E. (2009)
Comparative study of sorption and permeation techniques for the determination of heptane and toluene transport in polyethylene membranes
in Journal of membrane science (Print); Elsevier B.V., Amsterdam (Belgio)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Friess,K., Jansen, J.C., Vopicka, O., Randová, A., Hynek, V., Sípek, M., Bartovská, L., Izák, P., Dingemans, m., Dewulf, J., Van Langenhove, H., Drioli E. (literal)
- Pagina inizio
- Pagina fine
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- Rivista
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- Doi:10.1016/j.memsci.2009.04.030 (literal)
- Note
- Scopus (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Physical Chemistry, Institute of Chemical Technology, Technická 5, 166 28 Prague 6, Czech Republic
Institute of Chemical Process Fundamentals, Rozvojová 2, 165 02 Prague 6, Czech Republic
Research Group EnVOC, Faculty of Bioscience Engineering, Ghent University, Coupure links 653, 9000, Ghent, Belgium
Institute for Membrane Technology, ITM-CNR, Via P. Bucci 17/C, 87030 Rende (CS), Italy. (literal)
- Titolo
- Comparative study of sorption and permeation techniques for the determination of heptane and toluene transport in polyethylene membranes (literal)
- Abstract
- A comprehensive study of the mass transport of two volatile organic compounds (VOCs) heptane and toluene and their binary mixtures through dense semicrystalline low density polyethylene membranes (LDPE) at 25 æC is presented. The use of the widest possible concentration range (VOCs activity of 0.0011 at given temperature) and a set of four different experimental techniques enabled to reveal differences between permeation and sorption of studied vapours and to clarify the effect of feed and instantaneous VOCs concentration inside the LDPE membrane. The differential flow permeation method and fixedvolume pressure increase method were used for pure and binary vapour permeation while sorption measurements (from liquid and vapour phases)were performed gravimetrically and by the Vapour Phase Calibration technique (VPC).
This work is the first and unique comparative study on a so wide range of vapour activities and a so vast number of different techniques, giving important insight into the transport phenomena themselves and on how results are affected by the specific technique used. Results are demonstrated and discussed in detail on the basis of a pair of penetrants with different physico-chemical properties and molecular shape (toluene vs. heptane). Information about differences between concentration dependent permeation and sorption, coupling effect, molecular clustering and polymersolvent interactions is reported as well.
The establishment of specific concentration profiles inside the LDPE membrane during permeation and sorption experiments evoke time-dependent structure changes of the LDPE matrix and such chain reorganisations consequently influence the transport parameters and they are also related to a certain form of high concentration-evoked molecular aggregation (clustering). X-Ray diffraction measurements excluded that the observed phenomena could be due to significant irreversible changes in the crystallinity of the material. Toluene and heptane favourably influence one anothers transport and consequently both sorption and permeation experiments reveal a distinct coupling effect. Permeation experiments show a gradual increase of the integral diffusion with increasing vapour activity whereas VPC and gravimetric sorption analysis find a maximum around activity a = 0.7. This difference is due to the deviation from Fickian behaviour at high activity and to fundamental differences in the measurement principle. (literal)
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