Tracing Coffee Tabletop Traces

Jork Leiterer, Franziska Emmerling*, Ulrich Panne, Wolfgang Christen and Klaus Rademann*
BAM Federal Institute for Materials Research and Testing, Richard-Willsttter-Strasse 11, 12489 Berlin, Germany, and Institut fr Chemie, Humboldt-Universitt zu Berlin, Brook-Taylor-Strasse 2, 12489 Berlin, Germany
Langmuir, 2008, 24 (15), pp 7970–7978
DOI: 10.1021/la800768v
Publication Date (Web): June 26, 2008
Copyright © 2008 American Chemical Society

BAM Federal Institute for Materials Research and Testing.

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* Corresponding authors. (K.R.) Phone: +49 (0)30 20935561, fax: +49 (0)30 20935559, e-mail: klaus.rademann@chemie.hu-berlin.de; (F.E.) phone: +49 (0)30 8104 1133, fax: +49 (0)30 81041137, e-mail: franziska.emmerling@bam.de.
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Humboldt-Universitt zu Berlin.

Abstract

Abstract Image

Crystallization processes under different conditions are of fundamental interest in chemistry, pharmacy, and medicine. Therefore, we have studied the formation of micro- and nanosized crystals using water−caffeine (1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione) solutions under ambient conditions as a relevant model system. When droplets of an aqueous caffeine solution evaporate and eventually dry on surfaces (glass, polystyrene, and polyester), stable “coffee tabletop” rings with a perimeter of typically 3 mm are formed after 20 to 50 min. Using a micro focus X-ray beam available at the BESSY μSpot-beamline, the fine structure of different caffeine needles can be distinguished. Unexpectedly, both crystal modifications (α- and β-caffeine) are present, but locally separated in these rings. Furthermore, AFM studies reveal the presence of even smaller particles on a nanometer length scale. To eliminate influences of surface irregularities from the crystallization process, acoustic levitation of liquid samples was employed. Such levitated droplets are trapped in a stable position and only surrounded by air. The solvent in an ultrasonically levitated drop evaporates completely, and the resulting crystallization of caffeine was followed in situ by synchrotron X-ray diffraction. In this case, the diffraction pattern is in accordance with pure α-caffeine and does not indicate the formation of the room temperature polymorph β-caffeine. Hence, our investigations open new vistas that may lead to a controlled formation of cocrystals and novel polymorphs of micro- and nanocrystalline materials, which are of relevance for fundamental studies as well as for pharmaceutical and medical applications.

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History

  • Published In Issue August 05, 2008
  • Article ASAPJune 26, 2008
  • Received: March 11, 2008
    Revised: May 13, 2008

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