@article{XieJelicicWangetal.2010, author = {Xie, Zai-Lai and Jelicic, Aleksandra and Wang, Feipeng and Rabu, Pierre and Friedrich, Alwin and Beuermann, Sabine and Taubert, Andreas}, title = {Transparent, flexible, and paramagnetic ionogels based on PMMA and the iron-based ionic liquid 1-butyl-3- methylimidazolium tetrachloroferrate(III) [Bmim][FeCl4]}, issn = {0959-9428}, doi = {10.1039/C0jm01733g}, year = {2010}, abstract = {The iron-containing ionic liquid (IL) 1-butyl-3-methylimidazolium tetrachloroferrate(III) [Bmim][FeCl4] has been used as a building block in the synthesis of transparent, ion-conducting, and paramagnetic ionogels. UV/Vis spectroscopy shows that the coordination around the Fe(III) ion does slightly change upon incorporation of the IL into PMMA. The thermal stability of the PMMA increases significantly with IL incorporation. In particular, the onset weight loss observed at ca. 265 degrees C for pure PMMA is completely suppressed. The ionic conductivity shows a strong temperature dependence and increases with increasing IL weight fractions. The magnetic properties are similar to those reported for the pure IL and are not affected by the incorporation into the PMMA matrix. The resulting ionogel is thus an interesting prototype for soft, flexible, and transparent materials combining the mechanical properties of the matrix with the functionality of the metal-containing IL, such as magnetism.}, language = {en} } @article{JelicicYasinBeuermann2011, author = {Jelicic, Aleksandra and Yasin, Muttaqin and Beuermann, Sabine}, title = {Toward the description and prediction of solvent induced variations in Methacrylate Propagation Rate Coefficients on the basis of Solvatochromic Parameters}, series = {Macromolecular reaction engineering}, volume = {5}, journal = {Macromolecular reaction engineering}, number = {5-6}, publisher = {Wiley-Blackwell}, address = {Malden}, issn = {1862-832X}, doi = {10.1002/mren.201000058}, pages = {232 -- 242}, year = {2011}, abstract = {Benzyl methacrylate (BzMA) propagation rate coefficients, k(p), were determined in ionic liquids and common organic solvents via pulsed-laser polymerizations with subsequent polymer analysis by size-exclusion chromatography (PLP-SEC). The aim of the work is to gain a deeper understanding of the solvent influence on k(p) and to develop a general correlation between solvent-induced variations in k(p) and solvent properties. Applying a linear solvation energy relationship (LSER), which correlates k(p) to solvent solvatochromic parameters, suggests that dipolarity/polarizability determines the solvent influence on k(p). To compare the solvent influence on BzMA k(p) with data for methyl methacrylate, hydroxypropyl methacrylate, and 2-ethoxyethyl methacrylate normalized k(p) data were treated by a single LSER, providing a universal treatment of the solvent influence on the propagation kinetics of the four monomers. Further, the predictive capabilities of this universal correlation were tested with additional monomers from the methacrylate family.}, language = {en} } @article{SchmidtBehlLendleinetal.2014, author = {Schmidt, Christian and Behl, Marc and Lendlein, Andreas and Beuermann, Sabine}, title = {Synthesis of high molecular weight polyglycolide in supercritical carbon dioxide}, series = {RSC Advances}, volume = {4}, journal = {RSC Advances}, number = {66}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {2046-2069}, doi = {10.1039/c4ra06815g}, pages = {35099 -- 35105}, year = {2014}, abstract = {Polyglycolide (PGA) is a biodegradable polymer with multiple applications in the medical sector. Here the synthesis of high molecular weight polyglycolide by ring-opening polymerization of diglycolide is reported. For the first time stabilizer free supercritical carbon dioxide (scCO(2)) was used as a reaction medium. scCO(2) allowed for a reduction in reaction temperature compared to conventional processes. Together with the lowering of monomer concentration and consequently reduced heat generation compared to bulk reactions thermal decomposition of the product occurring already during polymerization is strongly reduced. The reaction temperatures and pressures were varied between 120 and 150 degrees C and 145 to 1400 bar. Tin(II) ethyl hexanoate and 1-dodecanol were used as catalyst and initiator, respectively. The highest number average molecular weight of 31 200 g mol(-1) was obtained in 5 hours from polymerization at 120 degrees C and 530 bar. In all cases the products were obtained as a dry white powder. Remarkably, independent of molecular weight the melting temperatures were always at (219 +/- 2)degrees C.}, language = {en} } @article{GoebelHesemannWeberetal.2009, author = {Goebel, Ronald and Hesemann, Peter and Weber, Jens and Moeller, El{\´e}onore and Friedrich, Alwin and Beuermann, Sabine and Taubert, Andreas}, title = {Surprisingly high, bulk liquid-like mobility of silica-confined ionic liquids}, issn = {1463-9076}, doi = {10.1039/B821833a}, year = {2009}, abstract = {Mesoporous silica monoliths were prepared by the sol - gel technique and. lled with 1-ethyl-3-methyl imidazolium [Emim]-X (X = dicyanamide [N(CN)(2)], ethyl sulfate [EtSO4], thiocyanate [SCN], and triflate [TfO]) ionic liquids (ILs) using a methanol-IL exchange technique. The structure and behavior of the ILs inside the silica monoliths were studied using X-ray scattering, nitrogen sorption, IR spectroscopy, solid-state NMR, and thermal analysis. DSC finds shifts in both the glass transition temperature and melting points (where applicable) of the ILs. Glass transition and melting occur well below room temperature. There is thus no conflict with the NMR and IR data, which show that the ILs are as mobile at room temperature as the bulk (not confined) ILs. The very narrow line widths of the NMR spectra suggest that the ILs in our materials have the highest mobility reported for confined ILs so far. As a result, our data suggest that it is possible to generate IL/silica hybrid materials (ionogels) with bulk-like properties of the IL. This could be interesting for applications in, e.g., the solar cell or membrane fields.}, language = {en} } @article{Beuermann2009, author = {Beuermann, Sabine}, title = {Solvent influence on propagation kinetics in radical polymerizations studied by pulsed laser initiated polymerizations}, issn = {1022-1336}, doi = {10.1002/marc.200900131}, year = {2009}, abstract = {The influence of the reaction medium (organic solvents, water, ionic liquids, supercritical CO2) on the propagation rate in radical polymerizations has very different causes, e.g., hindered rotational modes, hydrogen bonding or electron pair donor/acceptor interactions. Depending on the origin of the solvent influence propagation rate coefficients, k(P), may be enhanced by up to an order of magnitude associated with changes in the pre-exponential or the activation energy of k(P). In contrast, non-specific interactions, size and steric effects lead to rather small changes in the vicinity of the radical chain end and are reflected by modest variations in k(P).}, language = {en} } @article{Beuermann2009, author = {Beuermann, Sabine}, title = {Solvent influence on propagation kinetics in radical polymerizations studied by pulsed laser initiated polymerizations}, issn = {1022-1336}, year = {2009}, abstract = {The influence of the reaction medium (organic solvents, water, ionic liquids, supercritical CO2) on the propagation rate in radical polymerizations has very different causes, e.g., hindered rotational modes, hydrogen bonding, or electron pair donor / acceptor interactions. Depending on the origin of the solvent influence propagation rate coefficients, kp, may be enhanced by up to an order of magnitude associated with changes in the pre-exponential or the activation energy of kp. Contrary, non-specific interactions, size and steric effects lead to rather small changes in the vicinity of the radical chain end and are reflected by modest variations in kp.}, language = {en} } @article{SiegmannMoellerBeuermann2012, author = {Siegmann, Rebekka and M{\"o}ller, Eleonore and Beuermann, Sabine}, title = {Propagation rate coefficients for homogeneous phase VDF-HFP copolymerization in supercritical CO2}, series = {Macromolecular rapid communications}, volume = {33}, journal = {Macromolecular rapid communications}, number = {14}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1022-1336}, doi = {10.1002/marc.201200115}, pages = {1208 -- 1213}, year = {2012}, abstract = {For the first time, propagation rate coefficients, kp,COPO, for the copolymerizations of vinylidene fluoride and hexafluoropropene have been determined. The kinetic data was determined via pulsed-laser polymerization in conjunction with polymer analysis via size-exclusion chromatography, the PLP-SEC technique. The experiments were carried out in homogeneous phase with supercritical CO2 as solvent for temperatures ranging from 45 to 90 degrees C. Absolute polymer molecular weights were calculated on the basis of experimentally determined MarkHouwink constants. The Arrhenius parameters of kp,COPO vary significantly compared with ethene, which is explained by the high electronegativity of fluorine and less intra- and intermolecular interactions between the partially fluorinated macroradicals.}, language = {en} } @article{JelicicGarciaLoehmannsroebenetal.2009, author = {Jelicic, Aleksandra and Garcia, Nuria and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Beuermann, Sabine}, title = {Prediction of the ionic liquid influence on propagation rate coefficients in methyl methacrylate radical polymerizations based on Kamlet-Taft solvatochromic parameters}, issn = {0024-9297}, doi = {10.1021/ma9017907}, year = {2009}, language = {en} } @book{Beuermann2007, author = {Beuermann, Sabine}, title = {Polymerisation im Kohlendioxid : Antrittsvorlesung 2007-01-25}, publisher = {Univ.-Bibl.}, address = {Potsdam}, year = {2007}, abstract = {In ihrer Vorlesung zeigt Sabine Beuermann, unter welchen Bedingungen Kohlendioxid als Reaktionsmedium f{\"u}r die Herstellung von polymeren Materialien genutzt werden kann. Fluides Kohlendioxid ist ein attraktives Reaktionsmedium, da es ungiftig und nicht brennbar ist. Zudem leistet es einen wichtigen Beitrag zur Entwicklung nachhaltiger chemischer Prozesse, da durch den Einsatz von Kohlendioxid die Verwendung von organischen L{\"o}sungsmitteln vermieden werden kann.}, language = {de} } @article{VukicevicVukovicStoyanovetal.2012, author = {Vukicevic, Radovan and Vukovic, Ivana and Stoyanov, Hristiyan and Korwitz, Andreas and Pospiech, Doris and Kofod, Guggi and Loos, Katja and ten Brinke, Gerrit and Beuermann, Sabine}, title = {Poly(vinylidene fluoride)-functionalized single-walled carbon nanotubes for the preparation of composites with improved conductivity}, series = {Polymer Chemistry}, volume = {3}, journal = {Polymer Chemistry}, number = {8}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c2py20166f}, pages = {2261 -- 2265}, year = {2012}, abstract = {The surface of single-walled carbon nanotubes (SWCNTs) was functionalized with azide-terminated poly(vinylidene fluoride) (PVDF). Functionalization was confirmed by dispersibility, Raman spectroscopy, and thermogravimetric analyses. Raman spectra show disordering of the SWCNTs, thus, strongly suggesting that PVDF was covalently attached to SWCNTs. Functionalized SWCNTs were mixed with commercially available PVDF in a twin-screw extruder and thin films were obtained by melt-pressing. Films containing 0.5 and 1 wt\% PVDF-functionalized SWCNTs exhibited significantly improved electrical conductivity compared to PVDF films containing pristine SWCNTs.}, language = {en} }