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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University of Bath

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (9/9 displayed)

  • 2016Effects of process parameters on polyaniline nanofiltration membranes synthesis via phase inversion-immersion precipitation methodcitations
  • 2014General concepts in sustainable chemical processescitations
  • 2013Greener photocatalysts111citations
  • 2011Surface and Charge Transport Characterization of Polyaniline−Cellulose Acetate Composite Membranes95citations
  • 2011Membrane potential and impedance studies of polyaniline composite membranes: effects of membrane morphology18citations
  • 2010Photocatalysis with nanostructured zinc oxide thin films: the relationship between morphology and photocatalytic activity under oxygen limited and oxygen rich conditions and evidence for a Mars Van Krevelen mechanism126citations
  • 2009Polyaniline deposition site control on microporous mixed cellulose ester membranes3citations
  • 2009Control of polyaniline deposition on microporous cellulose ester membranes by in situ chemical polymerization31citations
  • 2009Membrane characterisation by SEM, TEM and ESEM: the implications of dry and wetted microstructure on mass transfer through integrally skinned polyimide nanofiltration membranes46citations

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Rohani, Rosiah
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Hyland, Margaret
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Scott, Janet L.
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Jones, Mark I.
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Shariffuddin, Jun Haslinda
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Hyland, Margaret M.
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Qaiser, Asif A.
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Ali, Arshid M.
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Emanuelsson, Emma
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Costello, Sarah
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See-Toh, Yoong Hsiang
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Turner, Adrian
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Livingston, Andrew G.
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Havill, Alice
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Co-Authors (by relevance)

  • Rohani, Rosiah
  • Hyland, Margaret
  • Scott, Janet L.
  • Jones, Mark I.
  • Shariffuddin, Jun Haslinda
  • Hyland, Margaret M.
  • Qaiser, Asif A.
  • Ali, Arshid M.
  • Emanuelsson, Emma
  • Costello, Sarah
  • See-Toh, Yoong Hsiang
  • Turner, Adrian
  • Livingston, Andrew G.
  • Havill, Alice
OrganizationsLocationPeople

article

Greener photocatalysts

  • Patterson, Darrell
  • Jones, Mark I.
  • Shariffuddin, Jun Haslinda
Abstract

This paper demonstrates for the first time the feasibility of utilizing waste mussel shells for the synthesis of hydroxyapatite, Ca10(PO4)6(OH)2 (denoted as HAP) to be used as a greener, renewable photocatalyst for recalcitrant wastewater remediation. HAP was synthesised from Perna Canaliculus (green-lipped mussel) shells using a novel pyrolysis-wet slurry precipitation process. The physicochemical properties of the HAP were characterized using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). The HAP produced was of comparable quality to commercial (Sulzer Metco) HAP. The synthesized HAP had good photocatalytic activity, whereby methylene blue (a model textile wastewater compound) and its azo dye breakdown products were degraded with an initial rate of 2.5 × 10−8 mol L−1 min−1. The overall azo dye degradation was nearly 54% within 6 hours and 62% within 24 hours in an oxygen saturated feed in a batch reactor using a HAP concentration of 2.0 g/L, methylene blue concentration of 5 mg/L, UV irradiation wavelength of 254 nm and a stirring speed of 300 rpm. The kinetics were well described by three first order reactions in series, reflecting the reaction pathway from methylene blue to azo dye intermediates, then to smaller more highly oxidised intermediates and finally degradation of the recalcitrants. The final two steps of the reaction had significantly slower rates than the initial step (rates constants of 6.2 × 10−3 min−1, 1.2 × 10−3 min−1 and approximately (due to limited data points) 1.6 × 10−4 min−1 for the first, second and third step respectively), which tie in with this mechanism, however it could also indicate that the reaction is either product inhibited and/or affected by catalyst deactivation. FTIR analysis of the post-reaction HAP revealed surface PO43− group loss. Since there is good photocatalytic activity with oxygen in limited and excess supply during the photoreaction, this indicates the possibility of lattice oxygen participation in the photocatalytic reaction, which needs to be characterised more fully. However, overall, these results indicate that the HAP derived from the mussel shells is a promising greener, renewable photocatalyst for the photocatalytic degradation of wastewater components.

Topics
  • pyrolysis
  • impedance spectroscopy
  • surface
  • compound
  • scanning electron microscopy
  • x-ray diffraction
  • Oxygen
  • precipitation
  • Fourier transform infrared spectroscopy