Publikace UTB
Repozitář publikační činnosti UTB

Impinging jet study of the deposition of colloidal particles on modified polycarbonate and poly(ethylene terephthalate) surfaces

Repozitář DSpace/Manakin

Zobrazit minimální záznam


dc.title Impinging jet study of the deposition of colloidal particles on modified polycarbonate and poly(ethylene terephthalate) surfaces en
dc.contributor.author Lapčík, Lubomír
dc.contributor.author Fraštík, Michal
dc.contributor.author Lapčíková, Barbora
dc.relation.ispartof International Journal of Heat and Mass Transfer
dc.identifier.issn 0017-9310 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2012
utb.relation.volume 55
utb.relation.issue 5-6
dc.citation.spage 1513
dc.citation.epage 1518
dc.type article
dc.language.iso en
dc.publisher Pergamon Elsevier Science Ltd. en
dc.identifier.doi 10.1016/j.ijheatmasstransfer.2011.11.002
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0017931011006399
dc.subject Contact angles of wetting en
dc.subject Deposition kinetics en
dc.subject Impinging jet en
dc.subject Phospholipid layer en
dc.subject Poly(ethylene terephthalate) en
dc.subject Polycarbonate en
dc.subject Polystyrene particles en
dc.description.abstract Main focus of this study was on characterization of surface properties of virgin and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) phospholipid layer coated poly(ethylene terephthalate) (PET) and polycarbonate (PC) planar articles. Surface properties were followed measuring static contact angles of wetting by means of sessile drop method and deposition of negative polystyrene (PS) colloidal particles followed by impinging jet method at defined flow regimes. It was found that phospholipid coating of both studied samples (PET, PC) let to the vigorous increase of the surface free energy. For coated samples major part of the surface free energy was dominated by polar component in contrast to the non-treated materials. Here the dispersive component was dominating. Results of the deposition experiments of polystyrene particles of 3 μm diameter correspond with trends obtained by contact angle measurements, i.e. the surface treated materials exhibited higher surface activity reflected in increased particle deposition rates. Simultaneously there was confirmed the fact, that with increasing magnitude of the Reynolds number of the dispersion flux the higher deposition rates were observed. © 2011 Elsevier Ltd. All rights reserved. en
utb.faculty Faculty of Technology
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1002587
utb.identifier.rivid RIV/70883521:28110/12:43865399!RIV13-MSM-28110___
utb.identifier.rivid RIV/70883521:28610/12:43865399!RIV13-MSM-28610___
utb.identifier.obdid 43865403
utb.identifier.scopus 2-s2.0-84355162291
utb.identifier.wok 000300333700009
utb.identifier.coden IJHMA
utb.source j-scopus
dc.date.accessioned 2012-02-10T13:15:07Z
dc.date.available 2012-02-10T13:15:07Z
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Lapčík, Lubomír
utb.contributor.internalauthor Fraštík, Michal
utb.contributor.internalauthor Lapčíková, Barbora
utb.fulltext.affiliation Lubomír Lapčík Jr. *, Michal Fraštík, Barbora Lapčíková Centre of Polymer Systems, Faculty of Technology, Tomas Bata University in Zlin, nám. T.G. Masaryka 5555, 760 05 Zlín, Czech Republic Centre of Polymer Systems, Faculty of Technology, Tomas Bata University in Zlin, nám. T.G. Masaryka 5555, 760 05 Zlín, Czech Republic * Corresponding author. Tel.: +420 57 6035115; fax: +420 57 6035141. E-mail address: [email protected] (L. Lapčík Jr.).
utb.fulltext.dates Received 20 July 2011 Accepted 31 October 2011 Available online 13 December 2011
utb.fulltext.references [1] T.G.M. van de Ven, Colloidal Hydrodynamics, Academic Press, London, San Diego, 1989. [2] T. Da̧broś, T.G.M. van de Ven, A direct method for studying particle deposition onto solid surfaces, Colloid Polym. Sci. 261 (8) (1983) 694–707. [3] P. Warszyński, Coupling of hydrodynamic and electric interactions in adsorption of colloidal particles, Adv. Colloid Interface Sci. 84 (1) (2000) 47–142. [4] M. Kamiti, T.G.M. van de Ven, Impinging jet studies of the kinetics of deposition and dissolution of calcium carbonate particles, Colloids Surfaces A: Physicochem. Eng. Aspects 100 (1) (1995) 117–129. [5] A.J. Goldman, R.G. Cox, H. Brenner, Slow viscous motion of a sphere parallel to a plane wall—I motion through a quiescent fluid, Chem. Eng. Sci. 22 (4) (1967) 653. [6] T.G.M. van de Ven, S.J. Kelemen, Characterizing polymers with an impinging jet, J. Colloid Interface Sci. 181 (1) (1996) 118–123. [7] T. Da̧broś, T.G.M. van de Ven, Kinetics of coating by colloidal particles, J. Colloid Interface Sci. 89 (1) (1982) 232–244. [8] Z. Adamczyk, P. Warszyński, L. Szyk– Warszyńska, P. Weroński, Role of convection in particle deposition at solid surfaces, Colloids Surfaces A: Physicochem. Eng. Aspects 165 (1–3) (2000) 157–187. [9] Z. Adamczyk, B. Siwek, M. Zembala, P. Weroński, Kinetics of localized adsorption of colloid particles, Langmuir 8 (11) (1992) 2605–2610. [10] M. Kamiti, T. Da̧broś, T.G.M. van de Ven, Kinetics of surface coagulation, J. Colloid Interface Sci. 172 (2) (1995) 459–466. [11] L. Lapčík, B. Alince, T.G.M. van de Ven, J. Pulp Paper Sci. 21 (1) (1995) J19–24. [12] T.G.M. van de Ven, P. Warszyński, X. Wu, T. Da̧broś, Colloidal Particle Scattering: A New Method to Measure Surface Forces, Langmuir 10 (9) (1994) 3046–3056. [13] P. Warszyński, X. Wu, T.G.M. van de Ven, Electrokinetic lift force for a charged particle moving near a charged wall — a modified theory and experiment, Colloids Surfaces A: Physicochem. Eng. Aspects 140 (1–3) (1998) 183–198. [14] M. Kamiti, T.G.M. van de Ven, Measurement of spring constants of polyacrylamide chains bridging particles to a solid surface, Macromolecules 29 (4) (1996) 1191–1194. [15] Z. Adamczyk, B. Siwek, P. Warszyński, E. Musiał, Kinetics of particle deposition in the radial impinging-jet cell, J. Colloid Interface Sci. 242 (1) (2001) 14–24. [16] Z. Adamczyk, Particles at Interfaces. Interactions. Deposition, Structure, Academic Press, London, 2006. [17] L. Lapčík Jr., L. Lapčík, S. De Smedt, J. Demeester, P. Chabreček, Hyaluronan: preparation, structure, properties, and applications, Chem. Rev. 98 (8) (1998) 2663–2684. [19] D.Y. Kwok, D. Li, A.W. Neumann, Evaluation of the Lifshitz–van der Waals/acid–base approach to determine interfacial tensions, Langmuir 10 (4) (1994) 1323. [20] L. Lapčík Jr., K. Benešová, L. Lapčík, S. De Smedt, B. Lapčíková, Chemical modification of hyaluronic acid: alkylation, Int. J. Polymer Analysis Characterization 15 (8) (2010) 486–496. [21] L. Lapčík, K. Kuběna, A. Galatík, V. Kellö, General Physiol. Biophys. 9 (3) (1990) 419–429. [22] K. Liedermann, L. Lapčík, Chem. Papers 50 (4) (1996) 218–223. [23] L. Lapčík, J. Schurz, Photochemical degradation of hyaluronic acid by singlet oxygen, Colloid Polymer Sci. 269 (6) (1991) 633–635. [24] D.S. Argyropoulos, F. Morin, L. Lapčík, Magnetic field and temperature effects on the solid state proton spin-lattice relaxation time measurements of wood and pulps, Holzforschung 49 (2) (1995) 115–118. [25] J. Škvarla, T. Luxbacher, M. Nagy, M. Sisol, Relationship of surface hydrophilicity, charge, and roughness of PET foils stimulated by incipient alkaline hydrolysis, Appl. Materials Interfaces 2 (7) (2010) 2116–2127. [26] M. Jurak, E. Chibowski, Zeta potential and surface free energy changes of solidsupported phospholipid (DPPC) layers caused by the enzyme phospholipase A2 (PLA2), Adsorption 15 (2) (2009) 211–219. [27] M. Jurak, E. Chibowski, Wettability and topography of phospholipid DPPC multilayers deposited by spin-coating on glass, silicon, and mica slides, Langmuir 23 (20) (2007) 10156–10163.
utb.fulltext.sponsorship This article was created with support of Operational Program Research and Development for Innovations co-funded by the European Regional Development Fund (ERDF) and national budget of Czech Republic within the framework of the Centre of Polymer Systems project (reg. number CZ.1.05/2.1.00/03.0111).
utb.fulltext.projects CZ.1.05/2.1.00/03.0111
utb.fulltext.faculty Faculty of Technology
utb.fulltext.ou -
Find Full text

Soubory tohoto záznamu

Zobrazit minimální záznam