European Journal of Lipid Science and Technology

Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Cover image for Vol. 114 Issue 1

Special Issue: Fats and oils as renewable feedstock for the chemical industry

January 2012

Volume 114, Issue 1

Pages 1–99

  1. Cover Picture

    1. Top of page
    2. Cover Picture
    3. In this issue
    4. Contents
    5. Editorial
    6. Review Articles
    7. Research Articles
    1. Eur. J. Lipid Sci. Technol. 1/2012

      Article first published online: 11 JAN 2012 | DOI: 10.1002/ejlt.201290000

  2. In this issue

    1. Top of page
    2. Cover Picture
    3. In this issue
    4. Contents
    5. Editorial
    6. Review Articles
    7. Research Articles
    1. You have free access to this content
      In this issue

      Article first published online: 11 JAN 2012 | DOI: 10.1002/ejlt.201290001

  3. Contents

    1. Top of page
    2. Cover Picture
    3. In this issue
    4. Contents
    5. Editorial
    6. Review Articles
    7. Research Articles
    1. Eur. J. Lipid Sci. Technol. 1/2012

      Article first published online: 11 JAN 2012 | DOI: 10.1002/ejlt.201290002

  4. Editorial

    1. Top of page
    2. Cover Picture
    3. In this issue
    4. Contents
    5. Editorial
    6. Review Articles
    7. Research Articles
    1. You have free access to this content
      Fats and oils as renewable feedstock for the chemical industry (page 1)

      Jürgen O. Metzger and Michael A. R. Meier

      Article first published online: 11 JAN 2012 | DOI: 10.1002/ejlt.201100411

  5. Review Articles

    1. Top of page
    2. Cover Picture
    3. In this issue
    4. Contents
    5. Editorial
    6. Review Articles
    7. Research Articles
    1. Electrochemical conversion of fatty acids (pages 2–9)

      Hans J. Schäfer

      Article first published online: 11 OCT 2011 | DOI: 10.1002/ejlt.201100045

      Thumbnail image of graphical abstract

      Heterocoupling (cross-coupling) of two different fatty acids. Two different acids are coelectrolyzed. By using an excess of the cheaper acid, the more valuable acid can be incorporated to a higher extent into the product.

    2. Recent developments in dehydration of glycerol toward acrolein over heteropolyacids (pages 10–23)

      Andreas Martin, Udo Armbruster and Hanan Atia

      Article first published online: 5 DEC 2011 | DOI: 10.1002/ejlt.201100047

      Thumbnail image of graphical abstract

      Glycerol valorization routes toward intermediates and final products via different types of chemical transformations.

    3. Standardization of vegetable oils composition to be used as oleochemistry feedstock through a selective hydrogenation process (pages 24–30)

      Federica Zaccheria, Rinaldo Psaro, Nicoletta Ravasio and Paolo Bondioli

      Article first published online: 11 OCT 2011 | DOI: 10.1002/ejlt.201100044

      Thumbnail image of graphical abstract

      The effect of the standardization treatment on different oils.

  6. Research Articles

    1. Top of page
    2. Cover Picture
    3. In this issue
    4. Contents
    5. Editorial
    6. Review Articles
    7. Research Articles
    1. Chemical modifications of Sterculia foetida L. oil to branched ester derivatives (pages 31–48)

      Robert Manurung, Louis Daniel, Hendrik H. van de Bovenkamp, Teddy Buntara, Siti Maemunah, Gerard Kraai, I. G. B. N. Makertihartha, Antonius A. Broekhuis and Hero J. Heeres

      Article first published online: 27 DEC 2011 | DOI: 10.1002/ejlt.201100149

      Thumbnail image of graphical abstract

      The chemical modifications of Sterculia foetida L. oil to branched ester derivatives.

    2. Esters of maleinized fatty compounds as plasticizers (pages 49–54)

      Ursula Biermann, Anton Jungbauer and Jürgen O. Metzger

      Article first published online: 3 NOV 2011 | DOI: 10.1002/ejlt.201100136

      Thumbnail image of graphical abstract

      Unsaturated FAME (methyl calendulate (1) , methyl α-eleostearate (2), and methyl oleate(3) ), Diels-Alder adducts obtained from methyl calendulate and maleic anhydride (4) and from methyl α-eleostearate and maleic anhydride (5), ene adduct obtained from methyl oleate and maleic anhydride (6) and Admergin acid® (7).

    3. Lowering the boiling point curve of biodiesel by cross-metathesis (pages 55–62)

      Rowena E. Montenegro and Michael A. R. Meier

      Article first published online: 30 JUN 2011 | DOI: 10.1002/ejlt.201100026

      Thumbnail image of graphical abstract

      Product mixture resulting from the cross-metathesis of biodiesel with 1-hexene.

    4. Thermal characteristics of oleochemical carbonate binary mixtures for potential latent heat storage (pages 63–70)

      James A. Kenar

      Article first published online: 8 SEP 2011 | DOI: 10.1002/ejlt.201100043

      Thumbnail image of graphical abstract

      DSC curve for the eutectic 80:20 wt% binary mixture of dodecyl (1a) and tetradecyl (1b) carbonates. Heating rate 0.5°C/min.

    5. Polyurethanes with bio-based and recycled components (pages 71–83)

      Hynek Beneš, Tomáš Vlček, Renáta Černá, Jiřina Hromádková, Zuzana Walterová and Romana Svitáková

      Article first published online: 30 JUN 2011 | DOI: 10.1002/ejlt.201000123

      Thumbnail image of graphical abstract

      Scanning electron microscopy images of the prepared rigid polyurethane foams with no addition of the recycled polyol (0 wt%) and with 50 and 100 wt% of the ?sh oil-derived recycled polyols (top row) and 50, 75, and 100 wt% of dipropylene glycol -derived recycled polyol (bottom row).

    6. Synthesis of pseudo-telechelic diols by transesterification and thiol-ene coupling (pages 84–91)

      Myriam Desroches, Sylvain Caillol, Rémi Auvergne and Bernard Boutevin

      Article first published online: 23 AUG 2011 | DOI: 10.1002/ejlt.201100132

      Thumbnail image of graphical abstract

      Synthetic pathways toward pseudo-telechelic diols.

    7. Synthesis of novel stimuli-responsive polyglycerol-based hydrogels (pages 92–99)

      Somaieh Salehpour, Christopher J. Zuliani and Marc A. Dubé

      Article first published online: 26 OCT 2011 | DOI: 10.1002/ejlt.201100049

      Thumbnail image of graphical abstract

      The mechanism of cross-linking reaction between hydroxyl group of polyglycerol and epoxide group of PEGDE (cross-linker).

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