Moshe Narkis
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Moshe Narkis has a total of 66 co-authors. Here are the top co-authors by number of shared publications:
A. Siegmann
Department of Materials Engineering, Technion-Israel Institute of Technology, Technion City, Haifa, Israel
23 shared publications- Ran Yosef Suckeveriene
Department of Water Industry Engineering, Kinneret Academic College on the Sea of Galilee, Zemach 1513200, Israel
14 shared publications - Ester Segal
Department of Biotechnology and Food Engineering, Technion – Israel Institute of Technology, 3200003 Haifa, Israel
12 shared publications R. Tchoudakov
Department of Chemical Engineering Technion–lsrael Institute of Technology Haifa 32000 Israel
12 shared publicationsRoza Tchoudakov
Department of Chemical Engineering Technion‐IIT Haifa Israel
8 shared publicationsA. Tzur
Department of Chemical Engineering Technion–lsrael Institute of Technology Haifa 32000 Israel
6 shared publications
Latest Publications
- 1 January 2016
- Published by Walter de Gruyter GmbH
Literature review: conducting carbon nanotube/polyaniline nanocomposites
- 1 January 2016
- Published by Walter de Gruyter GmbH
Literature review: conducting carbon nanotube/polyaniline nanocomposites
- 29 April 2015
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 26 (7) , 889-897
Electro‐mechanical sensors based on conductive hybrid nanocomposites
- 29 April 2015
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 26 (7) , 889-897
Electro‐mechanical sensors based on conductive hybrid nanocomposites
- 30 September 2014
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 25 (12) , 1446-1453
Conductive elastomeric nanocomposites based on oxidation of aniline with silver nitrate via inverse emulsion polymerization
- 30 September 2014
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 25 (12) , 1446-1453
Conductive elastomeric nanocomposites based on oxidation of aniline with silver nitrate via inverse emulsion polymerization
- 5 September 2014
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 25 (12) , 1484-1491
Controlled migration of antifog additives from LLDPE compatibilized with LLDPE grafted maleic anhydride
- 5 September 2014
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 25 (12) , 1484-1491
Controlled migration of antifog additives from LLDPE compatibilized with LLDPE grafted maleic anhydride
- 3 June 2014
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 25 (11) , 1301-1306
Polymer/carbon nanofillers films fabricated by latex technology
This research presents a generic fabrication method for tailoring polymer/carbon nanofillers composites with controlled architecture and composition. Two types of common carbon nanofillers, i.e. multi‐walled carbon nanotubes (MWNTs) and graphene nanosheets, are finely dispersed in an aqueous dispersion of polyacrylate followed by a microfiltration process. The second step allows preserving the high dispersion level of the nanofillers within the polymer matrix in the resulting solid films/layers. This study aims to investigate the structure–property relationship of the polyacrylate/nanofiller films, fabricated by the combination of latex technology and microfiltration. The polyacrylate/MWNTs system is studied over the entire MWNTs composition (0 to 100 wt%) and is shown to exhibit a structural transition; from a nanocomposite structure, in which the nanotubes are dispersed within a continuous polymer matrix, to a porous MWNTs macrostructure containing segregated polymer domains. This structural transition is corroborated with the films‐specific surface area values and the mechanical properties versus the MWNTs content. The percolation threshold of the studied polyacrylate/MWNTs systems is obtained at MWNTs content of ~0.04 wt%, an order of magnitude lower compared with cast films, fabricated by conventional latex technology. Polyacrylate/graphene nanosheet nanocomposites that are fabricated using the same method also demonstrate a structural transition from nanofiller/polymer composite material to graphene macrostructures. Copyright © 2014 John Wiley & Sons, Ltd.
- 3 June 2014
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 25 (11) , 1301-1306
Polymer/carbon nanofillers films fabricated by latex technology
This research presents a generic fabrication method for tailoring polymer/carbon nanofillers composites with controlled architecture and composition. Two types of common carbon nanofillers, i.e. multi‐walled carbon nanotubes (MWNTs) and graphene nanosheets, are finely dispersed in an aqueous dispersion of polyacrylate followed by a microfiltration process. The second step allows preserving the high dispersion level of the nanofillers within the polymer matrix in the resulting solid films/layers. This study aims to investigate the structure–property relationship of the polyacrylate/nanofiller films, fabricated by the combination of latex technology and microfiltration. The polyacrylate/MWNTs system is studied over the entire MWNTs composition (0 to 100 wt%) and is shown to exhibit a structural transition; from a nanocomposite structure, in which the nanotubes are dispersed within a continuous polymer matrix, to a porous MWNTs macrostructure containing segregated polymer domains. This structural transition is corroborated with the films‐specific surface area values and the mechanical properties versus the MWNTs content. The percolation threshold of the studied polyacrylate/MWNTs systems is obtained at MWNTs content of ~0.04 wt%, an order of magnitude lower compared with cast films, fabricated by conventional latex technology. Polyacrylate/graphene nanosheet nanocomposites that are fabricated using the same method also demonstrate a structural transition from nanofiller/polymer composite material to graphene macrostructures. Copyright © 2014 John Wiley & Sons, Ltd.
- 25 October 2013
- Published by Wiley in Polymer Composites
- Vol. 35 (4) , 788-794
The structure and electro‐mechanical properties of novel hybrid CNT/PANI nanocomposites
Electrically conductive elastomeric nanocomposites containing carbon nanotubes (CNT) and polyaniline (PANI) are reported in the present investigation. The synthesis procedure included an in situ inverse emulsion polymerization of aniline doped with dodecylbenzene sulfonic acid (DBSA) in the presence of CNT and dissolved styrene‐isoprene‐styrene (SIS) block copolymer. The PANI synthesis step was carried out by applying ultrasonic energy. The dispersions obtained were processed by two methods: a recently developed precipitation‐filtration procedure, and a conventional drop‐cast procedure. The techniques developed resulted in homogeneous exfoliated PANI coated nanotubes within the elastomeric matrix. The presence of CNT/PANI in the SIS elastomeric matrix affects thermal, mechanical, and electrical properties of the nanocomposites. The formation of continuous three‐dimensional CNT/PANI networks prepared via the precipitation‐filtration method enhances the nanocomposite properties. Contrarily, the intermittent three‐dimensional network prepared by conventional drop‐cast method leads to inferior properties. Nanocomposites produced by both techniques are observed by HRSEM. The two processing techniques result in different structures, which affect the physical properties of the materials produced. A relatively low percolation threshold for both methods was determined. The Young's modulus of the SIS/CNT/PANI significantly increased in the presence of CNT. The precipitation‐filtration technique yields an improved nanocomposite product compared to the drop‐cast route. POLYM. COMPOS., 35:788–794, 2014. © 2013 Society of Plastics Engineers
- 25 October 2013
- Published by Wiley in Polymer Composites
- Vol. 35 (4) , 788-794
The structure and electro‐mechanical properties of novel hybrid CNT/PANI nanocomposites
Electrically conductive elastomeric nanocomposites containing carbon nanotubes (CNT) and polyaniline (PANI) are reported in the present investigation. The synthesis procedure included an in situ inverse emulsion polymerization of aniline doped with dodecylbenzene sulfonic acid (DBSA) in the presence of CNT and dissolved styrene‐isoprene‐styrene (SIS) block copolymer. The PANI synthesis step was carried out by applying ultrasonic energy. The dispersions obtained were processed by two methods: a recently developed precipitation‐filtration procedure, and a conventional drop‐cast procedure. The techniques developed resulted in homogeneous exfoliated PANI coated nanotubes within the elastomeric matrix. The presence of CNT/PANI in the SIS elastomeric matrix affects thermal, mechanical, and electrical properties of the nanocomposites. The formation of continuous three‐dimensional CNT/PANI networks prepared via the precipitation‐filtration method enhances the nanocomposite properties. Contrarily, the intermittent three‐dimensional network prepared by conventional drop‐cast method leads to inferior properties. Nanocomposites produced by both techniques are observed by HRSEM. The two processing techniques result in different structures, which affect the physical properties of the materials produced. A relatively low percolation threshold for both methods was determined. The Young's modulus of the SIS/CNT/PANI significantly increased in the presence of CNT. The precipitation‐filtration technique yields an improved nanocomposite product compared to the drop‐cast route. POLYM. COMPOS., 35:788–794, 2014. © 2013 Society of Plastics Engineers
- 14 September 2013
- Published by Wiley in Polymer Engineering & Science
- Vol. 54 (9) , 2023-2028
A novel methodology for controlled migration of antifog from thin polyolefin films
Transparent plastic films are widely used in agriculture as greenhouses covering and in the food industry as packaging films. The films are usually prepared by hydrophobic low polarity thermoplastics such as polyethylene (PE). In a greenhouse, the temperature and humidity are usually higher than the outside temperature and fog will appear on the inner surface of the PE film. Anti‐fogging (AF) additives are tensoactive materials, mainly nonionic surfactants, equalizing the PE and water surface tensions, thus creating a thin, continuous film of water rather than discrete droplets. In the present work, a new method of controlled migration of AF is described, by grafting AF molecules to the surface of submicron inorganic particles. Glycerides and fatty acids are used as AF. During the grafting reaction two fractions are formed: attached AF fraction to the inorganic particles' surface, a fraction which cannot be detached by extraction, and an unreacted, thus unattached AF fraction. Solvent extraction, FTIR and TGA measurements have confirmed the existence of the grafted AF molecules to the inorganic particle's surfaces. Aging tests, developed in the present work, have shown a significant decrease of the AF migration rate, thus confirming an extended duration of the anti‐fog's activity. POLYM. ENG. SCI., 54:2023–2028, 2014. © 2013 Society of Plastics Engineers
- 14 September 2013
- Published by Wiley in Polymer Engineering & Science
- Vol. 54 (9) , 2023-2028
A novel methodology for controlled migration of antifog from thin polyolefin films
Transparent plastic films are widely used in agriculture as greenhouses covering and in the food industry as packaging films. The films are usually prepared by hydrophobic low polarity thermoplastics such as polyethylene (PE). In a greenhouse, the temperature and humidity are usually higher than the outside temperature and fog will appear on the inner surface of the PE film. Anti‐fogging (AF) additives are tensoactive materials, mainly nonionic surfactants, equalizing the PE and water surface tensions, thus creating a thin, continuous film of water rather than discrete droplets. In the present work, a new method of controlled migration of AF is described, by grafting AF molecules to the surface of submicron inorganic particles. Glycerides and fatty acids are used as AF. During the grafting reaction two fractions are formed: attached AF fraction to the inorganic particles' surface, a fraction which cannot be detached by extraction, and an unreacted, thus unattached AF fraction. Solvent extraction, FTIR and TGA measurements have confirmed the existence of the grafted AF molecules to the inorganic particle's surfaces. Aging tests, developed in the present work, have shown a significant decrease of the AF migration rate, thus confirming an extended duration of the anti‐fog's activity. POLYM. ENG. SCI., 54:2023–2028, 2014. © 2013 Society of Plastics Engineers
- 15 July 2013
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 24 (8) , 758-763
A novel approach for preparation of conductive hybrid elastomeric nano‐composites
- 15 July 2013
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 24 (8) , 758-763
A novel approach for preparation of conductive hybrid elastomeric nano‐composites
- 10 April 2013
- Published by Springer Nature in MRS Proceedings
- Vol. 1505
Highly-Tunable Polymer/CNTs Nanostructures: A Rapid and Facile Approach for Controlled Architecture and Composition
- 10 April 2013
- Published by Springer Nature in MRS Proceedings
- Vol. 1505
Highly-Tunable Polymer/CNTs Nanostructures: A Rapid and Facile Approach for Controlled Architecture and Composition
- 17 August 2012
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 128 (3) , 2129-2135
Synthesis of hybrid polyaniline/carbon nanotubes nanocomposites in toluene by dynamic interfacial inverse emulsion polymerization under sonication
This work describes an empirical study of in situ interfacial dynamic inverse emulsion polymerization process under sonication of aniline in the presence of nine different types of carbon nanotubes (CNT) in toluene. The polymerization method described in this work is simple and very fast (5 min) compared to the other literature reports (3–12 h). During polymerization, CNT are coated with polyaniline (PANI) forming a core‐shell structure of nanowires as evidenced by transmission electron microscopy (TEM) and high‐resolution scanning microscopy (HRSEM). HRSEM images and surface resistivity imply that PANI coating of CNT leads to a remarkable improvement in separation and dispersion of CNT in toluene, which otherwise would have rapidly coagulate and settle. Two of the nine different CNT studied have shown the lowest surface resistivities. Films of uniform thickness were successfully produced (HRSEM of cross‐sections). The effect of film thickness on conductivity and optical properties is reported in the work. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013
- 17 August 2012
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 128 (3) , 2129-2135
Synthesis of hybrid polyaniline/carbon nanotubes nanocomposites in toluene by dynamic interfacial inverse emulsion polymerization under sonication
This work describes an empirical study of in situ interfacial dynamic inverse emulsion polymerization process under sonication of aniline in the presence of nine different types of carbon nanotubes (CNT) in toluene. The polymerization method described in this work is simple and very fast (5 min) compared to the other literature reports (3–12 h). During polymerization, CNT are coated with polyaniline (PANI) forming a core‐shell structure of nanowires as evidenced by transmission electron microscopy (TEM) and high‐resolution scanning microscopy (HRSEM). HRSEM images and surface resistivity imply that PANI coating of CNT leads to a remarkable improvement in separation and dispersion of CNT in toluene, which otherwise would have rapidly coagulate and settle. Two of the nine different CNT studied have shown the lowest surface resistivities. Films of uniform thickness were successfully produced (HRSEM of cross‐sections). The effect of film thickness on conductivity and optical properties is reported in the work. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013