Materials Map

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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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in Cooperation with on an Cooperation-Score of 37%

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Publications (1/1 displayed)

  • 2011Synthesis of caffeic acid molecularly imprinted polymer microspheres and high-performance liquid chromatography evaluation of their sorption properties50citations

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Segura-Carretero, Antonio
1 / 2 shared
Cormack, Peter
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Gomez-Romero, Maria
1 / 1 shared
Fernandez-Sanchez, Jorge F.
1 / 1 shared
Valero-Navarro, Angel
1 / 1 shared
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2011

Co-Authors (by relevance)

  • Segura-Carretero, Antonio
  • Cormack, Peter
  • Gomez-Romero, Maria
  • Fernandez-Sanchez, Jorge F.
  • Valero-Navarro, Angel
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article

Synthesis of caffeic acid molecularly imprinted polymer microspheres and high-performance liquid chromatography evaluation of their sorption properties

  • Fernandez-Gutierrez, Alberto.
  • Segura-Carretero, Antonio
  • Cormack, Peter
  • Gomez-Romero, Maria
  • Fernandez-Sanchez, Jorge F.
  • Valero-Navarro, Angel
Abstract

In the current work, a molecularly imprinted polymer (MIP) has been synthesized and used to enable the extn. of a naturally-occurring antioxidant from complex media.More specifically, we describe the first example of a caffeic acid (CA) MIP which has been synthesized in the form of well-defined polymer microspheres, and its use for the extn. of CA from fruit juice sample.The CA MIP was synthesized by pptn. polymn. using 4-vinylpyridine as functional monomer, divinylbenzene-80 as crosslinker and acetonitrile:toluene (75/25, vol./vol.) as porogen.The particle sizing and morphol. characterization of the polymers was carried out by means of SEM (narrow particle size distribution; ∼5 and 1.5 μm particle diams. for the MIP and NIP [non-imprinted polymer], resp.) and nitrogen sorption porosimetry (sp. surface areas of 340 and 350 m2 g-1, and specific pore vols. of 0.17 and 0.19 cm3 g-1 for the MIP and NIP, resp.).The polymers were evaluated further by batch rebinding expts., and from the derived isotherms their binding capacity and binding strength were detd. (no. of binding sites (N K) = 0.6 and 0.3 mmol g-1 for the MIP and NIP, resp., and apparent av. adsorption const. (K N) = 10.0 and 1.6 L mmol-1 for the MIP and NIP, resp.).To evaluate the mol. recognition character of the MIP it was packed into a stainless steel column (50 mm × 4.6 mm i.d.) and evaluated as an HPLC-stationary phase.The mobile phase compn., flow rate, and the elution profile were then optimized in order to improve the peak shape without neg. affecting the imprinting factor (IF).Very interesting, promising properties were revealed.The imprinting factor (IF) under the optimized conditions was 11.9.Finally, when the imprinted LC column was used for the selective recognition of CA over eight related compds., very good selectivity was obtained.This outcome enabled the direct extn. of CA in com. apple juice samples with recoveries in excess of 81% and, rather significantly, without any need for a clean-up step prior to the extn.

Topics
  • pore
  • surface
  • polymer
  • stainless steel
  • phase
  • scanning electron microscopy
  • Nitrogen
  • strength
  • porosimetry
  • High-performance liquid chromatography
  • elution