@article{AsawapiromBulutFarrelletal.2004, author = {Asawapirom, Udom and Bulut, F. and Farrell, Tony and Gadermaier, C. and Gamerith, S. and G{\"u}ntner, Roland and Kietzke, Thomas and Patil, S. and Piok, T. and Montenegro, Rivelino V. D. and Stiller, Burkhard and Tiersch, Brigitte and Landfester, Katharina and List, E. J. W. and Neher, Dieter and Torres, C. S. and Scherf, Ullrich}, title = {Materials for polymer electronics applications semiconducting polymer thin films and nanoparticles}, issn = {1022-1360}, year = {2004}, abstract = {The paper presents two different approaches to nanostructured semiconducting polymer materials: (i) the generation of aqueous semiconducting polymer dispersions (semiconducting polymer nanospheres SPNs) and their processing into dense films and layers, and (ii) the synthesis of novel semiconducting polyfluorene-block-polyaniline (PF-b-PANI) block copolymers composed of conjugated blocks of different redox potentials which form nanosized morphologies in the solid state}, language = {en} } @article{BechtholdTierschKoetzetal.1999, author = {Bechthold, Nina and Tiersch, Brigitte and Koetz, Joachim and Friberg, Stig E.}, title = {Structure Formation in polymer-modified liquid crystals}, year = {1999}, language = {en} } @article{BertzWoehlBruhnMietheetal.2013, author = {Bertz, Andreas and W{\"o}hl-Bruhn, Stefanie and Miethe, Sebastian and Tiersch, Brigitte and Koetz, Joachim and Hust, Michael and Bunjes, Heike and Menzel, Henning}, title = {Encapsulation of proteins in hydrogel carrier systems for controlled drug delivery influence of network structure and drug size on release rate}, series = {Journal of biotechnology}, volume = {163}, journal = {Journal of biotechnology}, number = {2}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0168-1656}, doi = {10.1016/j.jbiotec.2012.06.036}, pages = {243 -- 249}, year = {2013}, abstract = {Novel hydrogels based on hydroxyethyl starch modified with polyethylene glycol methacrylate (HES-P(EG)(6)MA) were developed as delivery system for the controlled release of proteins. Since the drug release behavior is supposed to be related to the pore structure of the hydrogel network the pore sizes were determined by cryo-SEM, which is a mild technique for imaging on a nanometer scale. The results showed a decreasing pore size and an increase in pore homogeneity with increasing polymer concentration. Furthermore, the mesh sizes of the hydrogels were calculated based on swelling data. Pore and mesh size were significantly different which indicates that both structures are present in the hydrogel. The resulting structural model was correlated with release data for bulk hydrogel cylinders loaded with FITC-dextran and hydrogel microspheres loaded with FITC-IgG and FITC-dextran of different molecular size. The initial release depended much on the relation between hydrodynamic diameter and pore size while the long term release of the incorporated substances was predominantly controlled by degradation of the network of the much smaller meshes.}, language = {en} } @article{BourgatTierschKoetzetal.2020, author = {Bourgat, Yannick and Tiersch, Brigitte and Koetz, Joachim and Menzel, Henning}, title = {Enzyme degradable polymersomes from chitosan-g-[poly-l-lysine-block-epsilon-caprolactone] copolymer}, series = {Macromolecular bioscience}, volume = {21}, journal = {Macromolecular bioscience}, number = {1}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1616-5187}, doi = {10.1002/mabi.202000259}, pages = {1 -- 9}, year = {2020}, abstract = {The scope of this study includes the synthesis of chitosan-g-[peptide-poly-epsilon-caprolactone] and its self-assembly into polymeric vesicles employing the solvent shift method. In this way, well-defined core-shell structures suitable for encapsulation of drugs are generated. The hydrophobic polycaprolactone side-chain and the hydrophilic chitosan backbone are linked via an enzyme-cleavable peptide. The synthetic route involves the functionalization of chitosan with maleimide groups and the preparation of polycaprolactone with alkyne end-groups. A peptide functionalized with a thiol group on one side and an azide group on the other side is prepared. Thiol-ene click-chemistry and azide-alkyne Huisgen cycloaddition are then used to link the chitosan and poly-epsilon-caprolactone chains, respectively, with this peptide. For a preliminary study, poly-l-lysin is a readily available and cleavable peptide that is introduced to investigate the feasibility of the system. The size and shape of the polymersomes are studied by dynamic light scattering and cryo-scanning electron microscopy. Furthermore, degradability is studied by incubating the polymersomes with two enzymes, trypsin and chitosanase. A dispersion of polymersomes is used to coat titanium plates and to further test the stability against enzymatic degradation.}, language = {en} } @article{BresselPrevostAppavouetal.2011, author = {Bressel, Katharina and Prevost, Sylvain and Appavou, Marie-Sousai and Tiersch, Brigitte and Koetz, Joachim and Gradzielski, Michael}, title = {Phase behaviour and structure of zwitanionic mixtures of perfluorocarboxylates and tetradecyldimethylamine oxide-dependence on chain length of the perfluoro surfactant}, series = {Soft matter}, volume = {7}, journal = {Soft matter}, number = {23}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c1sm05618b}, pages = {11232 -- 11242}, year = {2011}, abstract = {Phase behaviour and the mesoscopic structure of zwitanionic surfactant mixtures based on the zwitterionic tetradecyldimethylamine oxide (TDMAO) and anionic lithium perfluoroalkyl carboxylates have been investigated for various chain lengths of the perfluoro surfactant with an emphasis on spontaneously forming vesicles. These mixtures were studied at a constant total concentration of 50 mM and characterised by means of dynamic light scattering (DLS), electric conductivity, small-angle neutron scattering (SANS), viscosity, and cryo-scanning electron microscopy (Cryo-SEM). No vesicles are formed for relatively short perfluoro surfactants. The extension of the vesicle phase becomes substantially larger with increasing chain length of the perfluoro surfactant, while at the same time the size of these vesicles increases. Head group interactions in these systems play a central role in the ability to form vesicles, as already protonating 10 mol\% of the TDMAO largely enhances the propensity for vesicle formation. The range of vesicle formation in the phase diagram is not only substantially enlarged but also extends to shorter perfluoro surfactants, where without protonation no vesicles would be formed. The size and polydispersity of the vesicles are related to the chain length of the perfluoro surfactant, the vesicles becoming smaller and more monodisperse with increasing perfluoro surfactant chain length. The ability of the mixed systems to form well-defined unilamellar vesicles accordingly can be controlled by the length of the alkyl chain of the perfluorinated surfactant and depends strongly on the charge conditions, which can be tuned easily by pH-variation.}, language = {en} } @article{CouturierWischerhoffBerninetal.2016, author = {Couturier, Jean-Philippe and Wischerhoff, Erik and Bernin, Robert and Hettrich, Cornelia and Koetz, Joachim and Sutterlin, Martin and Tiersch, Brigitte and Laschewsky, Andre}, title = {Thermoresponsive Polymers and Inverse Opal Hydrogels for the Detection of Diols}, series = {Langmuir}, volume = {32}, journal = {Langmuir}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.6b00803}, pages = {4333 -- 4345}, year = {2016}, abstract = {Responsive inverse opal hydrogels functionalized by boroxole moieties were synthesized and explored as sensor platforms for various low molar mass as well as polymeric diols and polyols, including saccharides, glycopolymers and catechols, by exploiting the diol induced modulation of their structural color. The underlying thermoresponsive water-soluble copolymers and hydrogels exhibit a coil-to-globule or volume phase transition, respectively, of the LCST-type. They were prepared from oligoethylene oxide methacrylate (macro)monomers and functionalized via copolymerization to bear benzoboroxole moieties. The resulting copolymers represent weak polyacids, which can bind specifically to diols within an appropriate pH window. Due to the resulting modulation of the overall hydrophilicity of the systems and the consequent shift of their phase transition temperature, the usefulness of such systems for indicating the presence of catechols, saccharides, and glycopolymers was studied, exploiting the diol/polyol induced shifts of the soluble polymers' cloud point, or the induced changes of the hydrogels' swelling. In particular, the increased acidity of benzoboroxoles compared to standard phenylboronic acids allowed performing the studies in PBS buffer (phosphate buffered saline) at the physiologically relevant pH of 7.4. The inverse opals constructed of these thermo- and analyte-responsive hydrogels enabled following the binding of specific diols by the induced shift of the optical stop band. Their highly porous structure enabled the facile and specific optical detection of not only low molar mass but also of high molar mass diol/polyol analytes such as glycopolymers. Accordingly, such thermoresponsive inverse opal systems functionalized with recognition units represent attractive and promising platforms for the facile sensing of even rather big analytes by simple optical means, or even by the bare eye.}, language = {en} } @article{DiehlCernochZenkeetal.2010, author = {Diehl, Christina and Cernoch, Peter and Zenke, Ingrid and Runge, Heike and Pitschke, Rona and Hartmann, Juergen and Tiersch, Brigitte and Schlaad, Helmut}, title = {Mechanistic study of the phase separation/crystallization process of poly(2-isopropyl-2-oxazoline) in hot water}, issn = {1744-683X}, doi = {10.1039/C0sm00114g}, year = {2010}, abstract = {The kinetics of the crystallization of thermoresponsive poly(2-isopropyl-2-oxazoline) in water and the time- dependent evolution of the morphology were examined using wide-angle X-ray scattering and conventional and cryogenic scanning electron microscopy. Results indicate that a temperature-induced phase separation produces a bicontinuous polymer network-like structure, which with the onset of crystallization collapses into individual particles (1-2 mu m in diameter) composed of a porous fiber mesh. Nanofibers then preferentially form at the particle surface, thus wrapping the microspheres like a ball of wool. The particle morphology is severely affected by changes in temperature and less by the initial polymer concentration.}, language = {en} } @article{DolyaRojasKosmellaetal.2013, author = {Dolya, Natalya and Rojas, Oscar and Kosmella, Sabine and Tiersch, Brigitte and Koetz, Joachim and Kudaibergenov, Sarkyt}, title = {"One-Pot" in situ frmation of Gold Nanoparticles within Poly(acrylamide) Hydrogels}, series = {Macromolecular chemistry and physics}, volume = {214}, journal = {Macromolecular chemistry and physics}, number = {10}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1022-1352}, doi = {10.1002/macp.201200727}, pages = {1114 -- 1121}, year = {2013}, abstract = {This paper focuses on two different strategies to incorporate gold nanoparticles (AuNPs) into the matrix of polyacrylamide (PAAm) hydrogels. Poly(ethyleneimine) (PEI) is used as both reducing and stabilizing agent for the formation of AuNPs. In addition, the influence of an ionic liquid (IL) (i.e., 1-ethyl-3-methylimidazolium ethylsulfate) on the stability of the nanoparticles and their immobilization in the hydrogel is investigated The results show that AuNPs surrounded by a shell containing PEI and IL, synthesized according to the one-pot approach, are much better immobilized within the PAAm hydrogel. Hereby, the IL is responsible for structural changes in the hydrogel as well as the improved stabilization and embedding of the AuNPs into the polymer gel matrix.}, language = {en} } @article{FrascaRojasSalewskietal.2012, author = {Frasca, Stefano and Rojas, Oscar and Salewski, Johannes and Neumann, Bettina and Stiba, Konstanze and Weidinger, Inez M. and Tiersch, Brigitte and Leimk{\"u}hler, Silke and Koetz, Joachim and Wollenberger, Ursula}, title = {Human sulfite oxidase electrochemistry on gold nanoparticles modified electrode}, series = {Bioelectrochemistry : an international journal devoted to electrochemical aspects of biology and biological aspects of electrochemistry ; official journal of the Bioelectrochemical Society}, volume = {87}, journal = {Bioelectrochemistry : an international journal devoted to electrochemical aspects of biology and biological aspects of electrochemistry ; official journal of the Bioelectrochemical Society}, publisher = {Elsevier}, address = {Lausanne}, issn = {1567-5394}, doi = {10.1016/j.bioelechem.2011.11.012}, pages = {33 -- 41}, year = {2012}, abstract = {The present study reports a facile approach for sulfite biosensing, based on enhanced direct electron transfer of a human sulfite oxidase (hSO) immobilized on a gold nanoparticles modified electrode. The spherical core shell AuNPs were prepared via a new method by reduction of HAuCl4 with branched poly(ethyleneimine) in an ionic liquids resulting particles with a diameter less than 10 nm. These nanoparticles were covalently attached to a mercaptoundecanoic acid modified Au-electrode where then hSO was adsorbed and an enhanced interfacial electron transfer and electrocatalysis was achieved. UV/Vis and resonance Raman spectroscopy, in combination with direct protein voltammetry, are employed for the characterization of the system and reveal no perturbation of the structural integrity of the redox protein. The proposed biosensor exhibited a quick steady-state current response, within 2 s, a linear detection range between 0.5 and 5.4 mu M with a high sensitivity (1.85 nA mu M-1). The investigated system provides remarkable advantages in the possibility to work at low applied potential and at very high ionic strength. Therefore these properties could make the proposed system useful in the development of bioelectronic devices and its application in real samples.}, language = {en} } @article{GroboschSchildeTiersch2006, author = {Grobosch, Thomas and Schilde, Uwe and Tiersch, Brigitte}, title = {Abtrennung von Arsen und anderer Schwermetalle mit impr{\"a}gnierten Adsorberpolymeren - teil 2: Abtrennung von Blei, Kupfer, Nickel und Zink}, issn = {0009-286X}, doi = {10.1002/cite.200500171}, year = {2006}, language = {de} } @article{GrosskopfTierschKoetzetal.2019, author = {Großkopf, S{\"o}ren and Tiersch, Brigitte and Koetz, Joachim and Mix, Andreas and Hellweg, Thomas}, title = {Shear-Induced Transformation of Polymer-Rich Lamellar Phases to Micron-Sized Vesicles}, series = {Langmuir}, volume = {35}, journal = {Langmuir}, number = {8}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.8602786}, pages = {3048 -- 3057}, year = {2019}, abstract = {In the present work, we study the shear-induced transformation of polymer-rich lamellar phases into vesicles. The evolution of vesicle size is studied by different scattering techniques, rheology, and microscopy methods. The lamellar phase found in the system D2O/o-xylene/Pluronic PE9400/C(8)TAB can be fully transformed to multilamellar vesicles (MLVs) by applying shear. The size of the MLVs is proportional to the inverse square root of the shear rate. Hence, the polymer based quaternary system behaves similar to lamellar phases based on small surfactant molecules. Additionally, we found a growth effect leading to a size increase of the vesicles after shearing was stopped.}, language = {en} } @article{HaaseGrigorievMoehwaldetal.2010, author = {Haase, Martin F. and Grigoriev, Dmitry and Moehwald, Helmuth and Tiersch, Brigitte and Shchukin, Dmitry G.}, title = {Encapsulation of amphoteric substances in a pH-sensitive pickering emulsion}, issn = {1932-7447}, doi = {10.1021/Jp104052s}, year = {2010}, abstract = {Oil-in-water (o/w) Pickering emulsions stabilized with silica nanoparticles were prepared. Droplets of diethyl phthalate (oil phase) act as reservoirs for 8-hydroxyquinoline (8-HQ), which is used as (a) the hydrophobizing agent for the silica particles and (b) an encapsulated corrosion inhibitor for application in active feedback coatings. The hydrophobization of silica nanoparticles with 8-HQ is determined by the amount of this agent adsorbed on the nanoparticle surface. The latter is governed by the 8-HQ concentration in the aqueous phase, which in turn depends on the degree of protonation and fir ally on the pH. We observe three ranges of 8-HQ adsorption value with respect to nanoparticle hydophobization: (I) insufficient, (2) sufficient, and (3) excessive adsorption by the formation of an 8-HQ bilayer, where only case 2 leads to the necessary nanoparticle hydrophobization. Hence emulsions stable in a narrow pH window between pH 5.5 and 4.4 follow. Here functional molecules are sufficiently charged to compensate for the charges on silica nanoparticles to make them interfacially active and thus able to stabilize an emulsion but they are still to a large extent uncharged and thereby remain in the oil phase. The emulsification is reversible upon changing the pH to a value beyond the stability region.}, language = {en} } @article{HaaseGrigorievMoehwaldetal.2011, author = {Haase, Martin F. and Grigoriev, Dmitry and Moehwald, Helmuth and Tiersch, Brigitte and Shchukin, Dmitry G.}, title = {Nanoparticle modification by weak polyelectrolytes for pH-sensitive pickering emulsions}, series = {Langmuir}, volume = {27}, journal = {Langmuir}, number = {1}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/la1027724}, pages = {74 -- 82}, year = {2011}, abstract = {The affinity of weak polyelectrolyte coated oxide particles to the oil-water interface can be controlled by the degree of dissociation and the thickness of the weak polyelectrolyte layer. Thereby the oil in water (o/w) emulsification ability of the particles can be enabled. We selected the weak polyacid poly(methacrylic acid sodium salt) and the weak polybase poly(allylamine hydrochloride) for the surface modification of oppositely charged alumina and silica colloids, respectively. The isoelectric point and the pH range of colloidal stability of both particle-polyelectrolyte composites depend on the thickness of the weak polyelectrolyte layer. The pH-dependent wettability of a weak polyelectrolyte-coated oxide surface is characterized by contact angle measurements. The o/w emulsification properties of both particles for the nonpolar oil dodecane and the more polar oil diethylphthalate are investigated by measurements of the droplet size distributions. Highly stable emulsions can be obtained when the degree of dissociation of the weak polyelectrolyte is below 80\%. Here the average droplet size depends on the degree of dissociation, and a minimum can be found when 15 to 45\% of the monomer units are dissociated. The thickness of the adsorbed polyelectrolyte layer strongly influences the droplet size of dodecane/water emulsion droplets but has a less pronounced impact on the diethylphthalate/water droplets. We explain the dependency of the droplet size on the emulsion pH value and the polyelectrolyte coating thickness with arguments based on the particle-wetting properties, the particle aggregation state, and the oil phase polarity. Cryo-SEM visualization shows that the regularity of the densely packed particles on the oil-water interface correlates with the degree of dissociation of the corresponding polyelectrolyte.}, language = {en} } @article{HornemannEichertHoehletal.2022, author = {Hornemann, Andrea and Eichert, Diane Madeleine and Hoehl, Arne and Tiersch, Brigitte and Ulm, Gerhard and Ryadnov, Maxim G. and Beckhoff, Burkhard}, title = {Investigating Membrane-Mediated Antimicrobial Peptide Interactions with Synchrotron Radiation Far-Infrared Spectroscopy}, series = {ChemPhysChem : a European journal of chemical physics and physical chemistry}, volume = {23}, journal = {ChemPhysChem : a European journal of chemical physics and physical chemistry}, number = {4}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1439-4235}, doi = {10.1002/cphc.202100815}, pages = {11}, year = {2022}, abstract = {Synchrotron radiation-based Fourier transform infrared spectroscopy enables access to vibrational information from mid over far infrared to even terahertz domains. This information may prove critical for the elucidation of fundamental bio-molecular phenomena including folding-mediated innate host defence mechanisms. Antimicrobial peptides (AMPs) represent one of such phenomena. These are major effector molecules of the innate immune system, which favour attack on microbial membranes. AMPs recognise and bind to the membranes whereupon they assemble into pores or channels destabilising the membranes leading to cell death. However, specific molecular interactions responsible for antimicrobial activities have yet to be fully understood. Herein we probe such interactions by assessing molecular specific variations in the near-THz 400-40 cm(-1) range for defined helical AMP templates in reconstituted phospholipid membranes. In particular, we show that a temperature-dependent spectroscopic analysis, supported by 2D correlative tools, provides direct evidence for the membrane-induced and folding-mediated activity of AMPs. The far-FTIR study offers a direct and information-rich probe of membrane-related antimicrobial interactions.}, language = {en} } @article{JyotishkumarKoetzTierschetal.2009, author = {Jyotishkumar, P. and Koetz, Joachim and Tiersch, Brigitte and Strehmel, Veronika and oezdilek, Ceren and Moldenaers, Paula and H{\"a}ssler, R{\"u}diger and Thomas, Sabu}, title = {Complex phase separation in poly(acrylonitrile-butadiene-styrene)-modified epoxy/4,4 '-diaminodiphenyl sulfone blends : generation of new micro- and nanosubstructures}, issn = {1520-6106}, doi = {10.1021/Jp8094566}, year = {2009}, abstract = {The epoxy system containing diglycidyl ether of bisphenol A and 4,4'-diaminodiphenyl sulfone is modified with poly(acrylonitrile-butadiene-styrene) (ABS) to explore the effects of the ABS content on the phase morphology, mechanism of phase separation, and viscoelastic properties. The amount of ABS in the blends was 5, 10, 15, and 20 parts per hundred of epoxy resin (phr). Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were employed to investigate the final morphology of ABS-modified epoxy blends. Scanning electron microscopic studies of 15 phr ABS-modified epoxy blends reveal a bicontinuous structure in which both epoxy and ABS are continuous, with substructures of the ABS phase dispersed in the continuous epoxy phase and substructures of the epoxy phase dispersed in the continuous ABS phase. TEM micrographs of 15 phr ABS-modified epoxy blends confirm the results observed by SEM. TEM micrographs reveal the existence of nanosubstructures of ABS in 20 phr ABS-modified epoxy blends. To the best of our knowledge, to date, nanosubstructures have never been reported in any epoxy/thermoplastic blends. The influence of the concentration of the thermoplastic on the generated morphology as analyzed by SEM and TEM was explained in detail. The evolution and mechanism of phase separation was investigated in detail by optical microscopy (OM) and small-angle laser light scattering (SALLS). At concentrations lower than 10 phr the system phase separates through nucleation and growth (NG). However, at higher concentrations, 15 and 20 phr, the blends phase separate through both NG and spinodal decomposition mechanisms. On the basis of OM and SALLS, we conclude that the phenomenon of complex substructure formation in dynamic asymmetric blends is due to the combined effect of hydrodynamics and viscoelasticity. Additionally, dynamic mechanical analysis was carried out to evaluate the viscoelastic behavior of the cross-linked epoxy/ABS blends. Finally, apparent weight fractions of epoxy and ABS components in epoxy- and ABS-rich phases were evaluated from T-g analysis.}, language = {en} } @article{KoethAppelhansRobertsonetal.2011, author = {Koeth, Anja and Appelhans, Dietmar and Robertson, Daniela and Tiersch, Brigitte and Koetz, Joachim}, title = {Use of weakly cationic dendritic glycopolymer for morphological transformation of phospholipid vesicles into tube-like networks}, series = {Soft matter}, volume = {7}, journal = {Soft matter}, number = {22}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c1sm06439h}, pages = {10581 -- 10584}, year = {2011}, abstract = {Using cationic polyelectrolytes with different molecular architectures, only hyperbranched poly(ethyleneimine) with maltose shell is suited to tailor the morphological transformation of anionic vesicles into tube-like networks. The interaction features of those materials partly mimic biological features of tubular proteins in nature.}, language = {en} } @article{KoethTierschAppelhansetal.2012, author = {Koeth, Anja and Tiersch, Brigitte and Appelhans, Dietmar and Gradzielski, Michael and C{\"o}lfen, Helmut and Koetz, Joachim}, title = {Synthesis of Core-Shell Gold Nanoparticles with Maltose-Modified Poly(Ethyleneimine)}, series = {Journal of dispersion science and technology}, volume = {33}, journal = {Journal of dispersion science and technology}, number = {1-3}, publisher = {Taylor \& Francis Group}, address = {Philadelphia}, issn = {0193-2691}, doi = {10.1080/01932691.2010.530084}, pages = {52 -- 60}, year = {2012}, abstract = {The synthesis of ultrafine gold nanoparticles in presence of maltose-modified hyperbranched poly(ethyleneimines) (PEI) is described. The polymer acted as both a reducing and stabilising agent in the particle formation process. The nanoparticles were characterized by means of dynamic light scattering (DLS), transmission electron microscopy (TEM), analytical ultracentrifugation (AUC), small-angle x-ray scattering (SAXS), and small-angle neutron scattering (SANS). The mechanism of nanoparticle formation can be described in two steps. The reduction process of the Au3+ ions located in the inner coil region of the hyperbranched PEI led to the formation of a compact gold core, and is accompanied by a collapse of the polymer coil. Therefore, in the subsequent reduction process a gold-polymer hybrid shell is formed. By using the PEI of higher molar mass, core-shell gold nanoparticles of about 3.6 nm size with a more narrow size distribution and special fluorescence behavior could be synthesized.}, language = {en} } @article{KoetzAndresKosmellaetal.2006, author = {Koetz, Joachim and Andres, S. and Kosmella, Sabine and Tiersch, Brigitte}, title = {BaSO4 nanorods produced in polymer-modified bicontinuous microemulsions}, issn = {0927-6440}, doi = {10.1163/156855406777408629}, year = {2006}, abstract = {The influence of the water soluble polymer poly(ethylene glycol) (PEG) on structure formation in the quasiternary system sodium dodecylsulfate (SDS)/pentanol-xylene/water was checked by means of conductometry, rheology, and micro differential calorimetry. The polymer induces the formation of an isotropic phase channel between the o/w and w/o microemulsion. The transition from the normal as well as from the inverse micellar to the bicontinuous phase range can be detected by conductometry, rheology as well as micro-DSC. As a result of polymer-surfactant interactions, the spontaneous curvature of the surfactant film is changed and a sponge phase is formed. The bicontinuous phase is characterized by a moderate shear viscosity, a Newtonian flow behaviour, and the disappearence of interphasal water in the heating curve of the micro-DSC. When the polymer-modified bicontinuous phase is used as a template phase for the nanoparticle formation, spherical BaSO4 nanoparticles were formed. During the following solvent evaporation process the primarily formed spherical nanoparticles aggregate to nanorods and triangular structures due to the non-restriction of the bicontinuous template phase in longitudinal direction}, language = {en} } @article{KoetzBahnemannLucasetal.2004, author = {Koetz, Joachim and Bahnemann, Jennifa and Lucas, Gordon and Tiersch, Brigitte and Kosmella, Sabine}, title = {Polyelectrolyte-modified microemulsions as new templates for the formation of nanoparticles}, issn = {0927-7757}, year = {2004}, abstract = {The paper is focused on the formation and redispersion of monodisperse BaSO4 nanoparticles in polyelectrolyte- modified microemulsions. It is shown that a cationic polyelectrolyte of low molar mass, e.g. poly(dially1dimethylammonium chloride) (PDADMAC), can be incorporated into the individual inverse microemulsion droplets (L2 phase) consisting of heptanol, water, and an amphoteric surfactant with a sulfobetaine head group. These PDADMAC- filled microemulsion droplets can be successfully used as a template phase for the nanoparticle formation. The monodisperse BaSO4 nanoparticles are produced by a simple mixing procedure and can be redispersed after solvent evaporation without a change in particle dimensions. Dynamic and electrophoretical light scattering in combination with sedimentation experiments in the analytical Ultracentrifuge of the redispersed powder show polyelectrolyte-stabilized nanoparticles with diameters of about 6 nm. The polyelectrolyte shows a "size control effect", which can be explained by the polyelectrolyte-surfactant interactions in relation to the polyelectrolyte-nanoparticle interactions during the particle growth, solvent evaporation and redispersion process. However, the approach used here opens away to produce different types of polyelectrolyte-stabilized nanoparticles (including rare metals, semiconductors, carbonates or oxides) of very small dimensions. (C) 2004 Elsevier B.V. All rights reserved}, language = {en} } @article{KoetzBeitzKosmellaetal.2000, author = {Koetz, Joachim and Beitz, Toralf and Kosmella, Sabine and Tiersch, Brigitte}, title = {Polymer-modified microemulsions}, year = {2000}, language = {en} }