Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Al-Malaika, Sahar

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Aston University

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (18/18 displayed)

  • 2021Influence of anti-ageing compounds on rheological properties of bitumen28citations
  • 2021Effect of processing conditions and catalyst type on the thermal oxidative degradation mechanisms and melt stability of metallocene and Ziegler‐catalyzed ethylene‐1‐hexene copolymers5citations
  • 2021New and novel stabilisation approach for radiation-crosslinked Ultrahigh Molecular Weight Polyethylene (XL-UHMWPE) targeted for use in orthopeadic implants14citations
  • 2020Photo-stabilization of biopolymers-based nanocomposites with UV-modified layered silicates6citations
  • 2017Novel strategic approach for the thermo- and photo-oxidative stabilization of polyolefin/clay nanocomposites15citations
  • 2017Novel strategic approach for the thermo- and photo- oxidative stabilization of polyolefin/clay nanocomposites15citations
  • 2017Thermo-oxidative stabilization of poly(lactic acid)-based nanocomposites through the incorporation of clay with in-built antioxidant activity16citations
  • 2015Novel organo-modifier for thermally-stable polymer-layered silicate nanocomposites37citations
  • 2013Influence of processing and clay type on nanostructure and stability of polypropylene-clay nanocomposites23citations
  • 2011Effect of contact surfaces on the thermal and photoxidation of dehydrated castor oil4citations
  • 2010Reactive processing of polymers20citations
  • 2009Effect of extrusion and photo-oxidation on polyethylene/clay nanocomposites92citations
  • 2009Reactive processing of polymers: structural characterization of products by 1H and 13C NMR spectroscopy for glycidyl methacrylate grafting onto EPR in the absence and presence of a reactive comonomer13citations
  • 2008Special issue of PDS - Based on PDDG meeting, Aston University, September 2007, in honour of Professor Norman Billinghamcitations
  • 2006Metallocene ethylene-1-octene copolymers36citations
  • 2005Polymer degradation and stability1citations
  • 2004Perspectives in stabilisation of polyolefins50citations
  • 2003Oxidative degradation and stabilisation of polymers41citations

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Co-Authors (by relevance)

  • Zhang, Yuqing
  • Omairey, Eman
  • Gao, Yangming
  • Sheena, Husam
  • Issenhuth, Sylvie
  • Daraz, Umar
  • Jefferies, Chris
  • Sheena, H. H.
  • Dintcheva, Nadka Tz
  • Arrigo, Rossella
  • Morici, Elisabetta
  • Dintcheva, Nadka Tzankova
  • Masarati, E.
  • Fischer, D.
  • Dole, H.
  • Stirling, T.
  • Sharples, M.
  • Doudin, Khalid
  • Eddiyanto, Eddy
  • Dintcheva, Nadka
  • Mantia, Francesco P. La
  • Ahmad, Azhar
  • Allen, Norman S.
  • Watson, H.
  • Peng, X.
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article

Effect of processing conditions and catalyst type on the thermal oxidative degradation mechanisms and melt stability of metallocene and Ziegler‐catalyzed ethylene‐1‐hexene copolymers

  • Issenhuth, Sylvie
  • Daraz, Umar
  • Al-Malaika, Sahar
Abstract

Polyolefins have traditionally been polymerized via the heterogeneous Ziegler Natta (Z-N) catalysts since their discovery in the 1950s, but the later developments of the homogeneous single site metallocene/methylaluminoxane (MAO) catalysts have opened the possibility for the synthesis of polyolefin polymers and copolymers (commercialized in the 1990s) with highly defined microstructure and great degree of control of their molecular architecture resulting in some unique beneficial properties compared to their Z-N counterparts. The main aim of the work reported here was to examine critically the effects of the processing conditions during multipass extrusions on the molecular and rheological characteristics of metallocene-catalyzed linear low density polyethylene and a Ziegler-Natta-based counterpart polymer and on the thermoxidative (in the melt) stability of their melts and their stabilization. Both polymers examined here were based on ethylene-1-hexene copolymers and produced by the same manufacturer with similar density and melt index (MI) values. The melt stability and rheological properties of the polymers were determined from melt flow and capillary rheometric measurements. The molecular characteristics were investigated using GPC for molecular weight determination, 13C-NMR for short chain branching, 1H-NMR and FTIR for the type and concentration of unsaturation groups, FTIR for carbonyl-containing compounds and chemical analysis for hydroperoxide determination. The processibility of the two polymers was compared through examination of different processing conditions (die temperatures 210–285°C, screw speeds 50–200 rpm) used for a multipass extrusion process. Further, the effects of the processing conditions on the melt thermoxidation of the differently catalyzed LLDPE polymers were investigated. The results demonstrated that both the catalyst type and the processing conditions have a great effect on both the rheological and the themoxidative behavior of the polymers as well as on the balance between the competing oxidative reactions taking place in the polymer melt, for example, chain scission and crosslinking reactions. The results obtained for the different multipass extrusion conditions of the two polymers have illustrated clearly that the degradation mechanisms during their melt processing are substantially different. The melt degradation route of the Ziegler-catalyzed polymer was shown to be dominated by chain scission reactions under all the processing conditions examined, and more so at the higher shear rates and temperatures. By contrast, the evidence clearly showed that the metallocene-catalyzed polymer gave rise to crosslinking reactions that predominated even under the more severe processing conditions, that is, higher temperatures and shear rates.

Topics
  • density
  • impedance spectroscopy
  • compound
  • melt
  • extrusion
  • molecular weight
  • copolymer
  • Nuclear Magnetic Resonance spectroscopy