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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-17T12:16:12Z</responseDate> <request identifier=oai:HAL:hal-01683214v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-01683214v1</identifier> <datestamp>2018-01-16</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:chim</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:CNRS</setSpec> <setSpec>collection:ENSC-MONTPELLIER</setSpec> <setSpec>collection:IEM</setSpec> <setSpec>collection:INC-CNRS</setSpec> <setSpec>collection:CHIMIE</setSpec> <setSpec>collection:UNIV-MONTPELLIER</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Molecular Weight Cut-Off and Structural Analysis of Vacuum-Assisted Titania Membranes for Water Processing</title> <creator>Yacou, Christelle</creator> <creator>Abd Jalil, Siti</creator> <creator>Wang, David</creator> <creator>Motuzas, Julius</creator> <creator>Smart, Simon</creator> <creator>Diniz da Costa, João</creator> <contributor>University of Queensland [Brisbane]</contributor> <contributor>Chimie des Matériaux - Connaissance et Valorisation (COVACHIMM) ; Université des Antilles et de la Guyane (UAG)</contributor> <contributor>Institut Européen des membranes (IEM) ; Centre National de la Recherche Scientifique (CNRS) - Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM) - Université Montpellier 2 - Sciences et Techniques (UM2) - Université de Montpellier (UM)</contributor> <description>International audience</description> <source>ISSN: 1996-1944</source> <source>EISSN: 1996-1944</source> <source>Materials</source> <publisher>MDPI</publisher> <identifier>hal-01683214</identifier> <identifier>https://hal.univ-antilles.fr/hal-01683214</identifier> <source>https://hal.univ-antilles.fr/hal-01683214</source> <source>Materials, MDPI, 2016, 9 (11), 〈10.3390/ma9110938〉</source> <identifier>DOI : 10.3390/ma9110938</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/ma9110938</relation> <language>en</language> <subject>[CHIM.MATE] Chemical Sciences/Material chemistry</subject> <subject>[CHIM.GENI] Chemical Sciences/Chemical engineering</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>This work investigates the structural formation and analyses of titania membranes (TM) prepared using different vacuum exposure times for molecular weight (MW) cut-off performance and oil/water separation. Titania membranes were synthesized via a sol-gel method and coated on macroporous alumina tubes followed by exposure to a vacuum between 30 and 1200 s and then calcined at 400 °C. X-ray diffraction and nitrogen adsorption analyses showed that the crystallite size and particle size of titania increased as a function of vacuum time. All the TM membranes were mesoporous with an average pore diameter of ~3.6 nm with an anatase crystal morphology. Water, glucose, sucrose, and polyvinylpyrrolidone with 40 and 360 kDa (PVP-40 kDa and PVP-360 kDa) were used as feed solutions for MW cut-off and hexadecane solution for oil filtration investigation. The TM membranes were not able to separate glucose and sucrose, thus indicating the membrane pore sizes are larger than the kinetic diameter of sucrose of 0.9 nm, irrespective of vacuum exposure time. They also showed only moderate rejection (20%) of the smaller PVP-40 kDa, however, all the membranes were able to obtain an excellent rejection of near 100% for the larger PVP-360 kDa molecule. Furthermore, the TM membranes were tested for the separation of oil emulsions with a high concentration of oil (3000 ppm), reaching high oil rejections of more than 90% of oil. In general, the water fluxes increased with the vacuum exposure time indicating a pore structural tailoring effect. It is therefore proposed that a mechanism of pore size tailoring was formed by an interconnected network of Ti-O-Ti nanoparticles with inter-particle voids, which increased as TiO2 nanoparticle size increased as a function of vacuum exposure time, and thus reduced the water transport resistance through the TM membranes. © 2016 by the authors.</description> <date>2016-11</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>