TY - CONF A1 - Elabshihy, Karim A1 - Kalinka, Gerhard T1 - Investigation of the time-dependent behavior of cnt-filled epoxy using nanoindentation N2 - Epoxy/Carbon nanotube (CNT) composites are interesting materials that could be used in a wide variety of applications. In this study, CNT contents of 0.25, 0.5, 1 and 2 wt% were used for reinforcing epoxy. A nanoindentation device and a temperature regulating system were developed in order to investigate the effect of CNTs on the time-dependent properties of epoxy using relaxations and creep tests on the nano scale. The relaxation tests showed a significant shift for the relaxation spectrum towards shorter times with introducing a low CNT content of 0.25 wt%. Additionally, creep tests showed that both the holding time at a constant load and the unloading velocity have a major effect on the contact stiffness. However, there was no effect for the CNTs on the creep behavior with contents lower than 1 wt%, which was related to the presence of a percolation threshold around this value. T2 - Nanobrücken 2013 CY - Dresden, Germany DA - 20.03.2013 KW - Epoxy KW - CNT KW - Time-dependent KW - Nanoindentation PY - 2013 AN - OPUS4-35533 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - de Camp, N. V. A1 - Kalinka, Gerhard A1 - Bergeler, J. T1 - Light-cured polymer electrodes for non-invasive EEG recordings N2 - We invented the first non-metallic, self-adhesive and dry biosignalling electrode. The PEDOT polymer electrode changes its aggregate state and conductivity by a light curing procedure. The electrode can be applied as a gel underneath hair without shaving. With the aid of blue light, the electrode can be hardened within a few seconds at the desired location on the scalp. The cured polymer electrode is highly conductive and can be applied on a very small location. Unlike other EEG electrodes, our electrode does not lose conductivity upon drying. Furthermore, our electrode strongly bonds to Skin and does not require any additional adhesive. Short circuits due to an outflow of gel are prevented with this technique. Therefore, the PEDOT polymer electrode is extremely well suited for applications that, up to now, have been challenging, such as non-invasive EEG recordings from awake and freely moving animals, EEG recordings from preterm babies in the neonatal intensive care unit or long-term recordings in the case of sleep monitoring or epilepsy diagnostics. We addressed two technical questions in this work. First, is the EEG recorded with polymer electrodes comparable to a standard EEG? Second, is it possible to record full-band EEGs with our electrodes? KW - Light curing KW - Polymer KW - Electric conductivity PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-459803 UR - https://rdcu.be/7aPD DO - https://doi.org/10.1038/s41598-018-32304-6 SN - 2045-2322 VL - 8 IS - 14041 SP - 1 EP - 9 PB - Nature Publishing Group CY - London AN - OPUS4-45980 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - THES A1 - Chung, Jaeun T1 - Nanoscale Characterization of Epoxy Interphase on Copper Microstructures N2 - The epoxy/metal interface regions are recognized as crucial for the mechanical reliability of composite materials. In particular, the spatial stress distribution is governed by modulus variations, which may result from the physical-chemical interactions between epoxy and the metal surface. The properties of the interphase between bulk polymer and metal were analyzed in nanometer scale. It was aimed to characterize the stiffness gradient of the polymeric interphase, which was formed by a thermoset being cured in contact with a metal surface. N2 - Die Grenzfläche zwischen Epoxid und Metall spielt für die mechanische Zuverlässigkeit des Verbundwerkstoffes (Composite) Epoxid/Metall eine wichtige Rolle. Insbesondere hängt die räumliche Verteilung mechanischer Spannungen von Variationen des Elastizitätsmoduls ab, die durch die physikalisch-chemischen Wechselwirkungen zwischen dem Epoxid und der Metalloberfläche hervorgerufen werden können. Daher wurden die Eigenschaften des Grenzbereichs (Interphase) zwischen dem Polymer, das nicht durch Grenzflächen-Wechselwirkungen beeinflusst wurde (Bulk-Polymer), und dem Metall auf der Nanometer-Skala analysiert. Hauptziel war es, die Steifigkeitsgradienten innerhalb der Epoxid-Interphase zu detektieren. Diese können durch die Gegenwart der Metall-Grenzfläche (Interface) hervorgerufen werden, die einen Einfluss auf den Prozess der Aushärtung zeigt. Die Rasterkraftmikroskopie (Scanning Force Microscopy, SFM) im Force Modulation Mode (FMM) erlaubt die hochauflösende Abbildung von Steifigkeitsvariationen. Die Ergebnisse aus der SFM-FMM wurden mit Konzentrationsprofilen aus der energiedispersiven Analyse von Röntgenstrahlen im Rasterelektronenmikroskop (REM-EDX) verglichen, als auch mit Relaxationskurven aus der dynamisch-mechanischen Analyse (DMA), die an Epoxid-Referenzproben durchgeführt wurde. Die untersuchten Verbundwerkstoff-Proben bestanden aus Epoxid und Kupfer. Es wurde Elektronstrahl-Lithographie (EBL) in Verbindung mit der Lift-off Technik verwendet, um Kupfer-Mikroelektroden auf einem Silizium-Wafer herzustellen. Danach wurde die Mischung aus Epoxidharz und Amin-Härter in der Gegenwart der Kupfer-Mikroelektroden ausgehärtet, wodurch ein Epoxid/Kupfer Verbundwerkstoff entstand. Es wurden zwei verschiedene Epoxid-Härter Systeme verwendet, um unterschiedliche Probentypen herzustellen. Eines bestand aus Diglycidyl-Ether des Bisphenol A (DGEBA) und einem modifizierten cycloaliphatischen Amin (EPIKOTE828 und EPIKURE F205 von Resolution Europe). Das andere bestand aus DGEBA und einem aromatischen Amin (DER332 von Dow Chemical und DDS von Fluka Chemikalien). SFM-FMM erlaubt es, die lokalen mechanischen Eigenschaften des Grenzbereichs zu beschreiben. Die neue Art der Probenpräparation ermöglicht es, eine an die Erfordernisse der SFM-FMM angepasste Glattheit der zu untersuchenden Oberfläche zu erzielen. Bei der SFM-FMM wird die vertikale Position der Probe moduliert und die dynamische Verbiegungsamplitude des SFM-Cantilevers gemessen, während sich die Spitze im Kontakt mit der Probenoberfläche befindet. Neben dem resultierenden Amplituden- und Phasensignal sind noch andere Kontraste verfügbar, wie Topographie, Auflagekraft und Lateralkraft. Diese ergänzenden Kontraste wurden dazu verwendet, die Kupfer-Grenzfläche zu identifizieren. Ferner dienten sie der Kontrolle der Qualität der SFMMessung. Insbesondere konnte gezeigt werden, dass von der Topographie induzierte Kontraste auftreten können, wenn ihre Neigung mehr als ~|3°| beträgt. Außerdem wurde die Morphologie der Oberfläche des Epoxids untersucht, die noppenartige Strukturen, so genannte „Noduln“, aufwies. Bei den gegebenen Aushärtungsbedingungen (Tg bei 80°C über 2 Stunden, Nachhärtung bei 130°C über 1 Stunde) betrug die Durchschnittsgröße der Noduln ~125 nm, und 90 Prozent der Noduln waren zwischen 75 und 200 nm groß. Das aus EPIKOTE828-EPIKURE F205 bestehende Epoxid-System bildete eine Interphase mit einer Breite von ~1,9 μm aus und der Punkt der niedrigsten Steifigkeit war in einem Abstand von ~0,4 μm vom Kupfer. Andererseits wies das DER332-DDS System eine Interphase mit einer Breite von ~2,3–4,0 μm auf. Es wurden verschiedenartige Steifigkeitsprofile festgestellt. Diese Ergebnisse zeigen, dass die Eigenschaften des metallinduzierten Grenzbereichs vom Epoxid-System abhängen. Die Steifigkeit in der Nähe von Kupfer (bis zu 0,2–0,25 μm Abstand) war deutlich höher als im Volumen des Epoxids. Sowohl die im REM als auch die im TEM durchgeführten EDX-Messungen zeigten, dass die Konzentration des Amins in der Nähe von Kupfer verringert ist. Die unter Verwendung von SFM-FMM gemessene Steifigkeit wurde mit dem Modulwert verglichen, der mittels DMA an Referenzproben wohldefinierter Amin-Epoxid Konzentrationsverhältnisse bestimmt wurde. Die gefundene Relation wurde im Rahmen eines Reaktions-Diffusions Modells interpretiert. Danach treten räumliche Schwankungen im Konzentrationsverhältnis von Amin und Epoxid auf, die zu Variationen in der Netzwerkstruktur des ausgehärteten Epoxidsführen und sich somit auch auf dessen mechanische Eigenschaften auswirken. T3 - BAM Dissertationsreihe - 15 KW - Nanoscale Characterization KW - Epoxy Interphase KW - Copper Microstructures PY - 2006 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-1435 SN - 978-3-86509-514-3 SN - 1613-4249 VL - 15 SP - 1 EP - 104 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-143 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Boro, I. A1 - Hinrichsen, G. A1 - Kalinka, Gerhard A1 - Hampe, Andreas A1 - Koßmehl, G. T1 - Zur Wechselstromleitfähigkeit von elektrisch leitfähgen Polymeren T2 - Präsentationsveranstaltung des Berliner Verbandes für Polymerforschung e.V. CY - Berlin, Germany DA - 1989-03-25 PY - 1989 AN - OPUS4-12126 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Blaker, Jonny A1 - Anthony, David B. A1 - Tang, Guang A1 - Shamsuddin, Siti-Ros A1 - Kalinka, Gerhard A1 - Shaffer, MIlo A1 - Abdolvand, Amin A1 - Bismarck, A. T1 - CARBON FIBRES WITH MODULATED PROPERTIES AND SHAPE ALONG THE FIBRE LENGTH T2 - 20th International Conference on Composite Materials - ICCM 20 CY - Copenhagen, Denmark DA - 2015-07-19 PY - 2015 AN - OPUS4-34454 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Blaker, J. J. A1 - Anthony, David B. A1 - Tang, G. A1 - Shamsuddin, S.-R. A1 - Kalinka, Gerhard A1 - Wienrich, Malte A1 - Abdolvand, Amin A1 - Shaffer, M. S. P. A1 - Bismarck, A. T1 - Property and shape modulation of carbon fibers using lasers N2 - An exciting challenge is to create unduloid-reinforcing fibers with tailored dimensions to produce synthetic composites with improved toughness and increased ductility. Continuous carbon fibers, the state-of-the-art reinforcement for structural composites, were modified via controlled laser irradiation to result in expanded outwardly tapered regions, as well as fibers with Q-tip (cotton-bud) end shapes. A pulsed laser treatment was used to introduce damage at the single carbon fiber level, creating expanded regions at predetermined points along the lengths of continuous carbon fibers, while maintaining much of their stiffness. The range of produced shapes was quantified and correlated to single fiber tensile properties. Mapped Raman spectroscopy was used to elucidate the local compositional and structural changes. Irradiation conditions were adjusted to create a swollen weakened region, such that fiber failure occurred in the laser treated Region producing two fiber ends with outwardly tapered ends. Loading the tapered fibers allows for viscoelastic energy dissipation during fiber pull-out by enhanced friction as the fibers plough through a matrix. In these tapered fibers, diameters were locally increased up to 53%, forming outward taper angles of up to 1.8°. The tensile strength and strain to failure of the modified fibers were significantly reduced, by 75% and 55%, respectively, ensuring localization of the break in the expanded region; however, the fiber stiffness was only reduced by 17%. Using harsher irradiation conditions, carbon fibers were completely cut, resulting in cottonbud fiber end shapes. Single fiber pull-out tests performed using these fibers revealed a 6.75-fold increase in work of pull-out compared to pristine carbon fibers. Controlled laser irradiation is a route to modify the shape of continuous carbon fibers along their lengths, as well as to cut them into controlled lengths leaving tapered or cotton-bud shapes. KW - Composite KW - Irradiation KW - Pull-out tests KW - Pulsed laser treatment KW - Single carbon fibers PY - 2016 DO - https://doi.org/10.1021/acsami.6b05228 SN - 1944-8244 SN - 1944-8252 VL - 8 IS - 25 SP - 16351 EP - 16358 PB - ACS Publications CY - 1155 Sixteenth Street, NW, Washington, DC 20036, USA AN - OPUS4-37699 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bismarck, A. A1 - Carreyette, S. A1 - Fontana, Q.P.V. A1 - Greenhalgh, E.S. A1 - Jacobsson, P. A1 - Johansson, P. A1 - Marczewski, M.J. A1 - Kalinka, Gerhard A1 - Kucernak, A. A1 - Shaffer, M.S. A1 - Shirshova, N. A1 - Steinke, J.H.G. A1 - Wienrich, Malte T1 - Multifunctional epoxy resin for structural supercapacitors N2 - Polymer-based electrolytes based on commercially available epoxy resins were prepared through the addition of a liquid electrolyte, a solution of a lithium salt in an ionic liquid. The polymer monoliths were characterized using impedance spectroscopy, 3-point bending test, scanning electron microscopy (SEM) and nitrogen adsorption (BET). The balance of ionic conductivity and flexural modulus is crucially dependent on the relative proportions of epoxy resin to electrolyte. Also the effect of the liquid electrolyte on curing kinetics and processing was assessed by complex viscosity measurements and differential scanning calorimetry (DSC). Only one out of the three resins investigated exhibited a significant acceleration effect. T2 - ECCM15 - 15th European conference on composite materials CY - Venice, Italy DA - 2012-06-24 KW - Multifunctional epoxy KW - Polymer electrolyte KW - Morphology KW - Ionic liquid PY - 2012 SN - 978-88-88785-33-2 SP - 1 EP - 8(?) AN - OPUS4-28694 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bismarck, A. A1 - Carreyette, Shuijin A1 - Fontana, Quentin P. A1 - Greenhalgh, E. A1 - Jacobsson, P. A1 - Johansson, P. A1 - Kalinka, Gerhard A1 - Wienrich, Malte T1 - Multifunctional Epoxy Resin for Structural Supercapacitors T2 - European Conference on Composite Materials 15 CY - Venice, Italy DA - 2012-06-24 PY - 2012 AN - OPUS4-27466 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Building macromolecular mimetics of cell constituents N2 - One of the holy grails in chemistry is to reconstruct some of life’s functions with synthetic materials. In this contribution, we demonstrate that “simple” macromolecular architectures such as dendritic amphiphiles, Janus dendrimers, thermoresponsive and hybrid organic-inorganic (co)polymers enable to mimic some of the functions of proteins for biomineralization, natural bactericides, biological membranes or the stimuli-responsive cytoskeleton. T2 - Makromolekulares Kolloquium Freiburg 2018 CY - Freiburg in Breisgau, Germany DA - 21.02.2018 KW - Thermoresponsive polymers KW - Cytoskeleton mimic PY - 2018 AN - OPUS4-44296 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad T1 - Upper critical solution temperature (UCST)-type thermoresponsive polymers from hydrogen-bonding monomers N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - Invited talk (Dr. Jean-Francois Lutz) Institut Charles Sadron CY - Strasbourg, France DA - 26.01.2018 KW - Thermoresponsive polymer KW - UCST-type polymer KW - H bonds KW - Diaminopyridine KW - Acrylamide PY - 2018 AN - OPUS4-44001 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad A1 - Ahmadi, Vahid T1 - Upper critical solution temperature (UCST)-type thermoresponsive polymers from hydrogen-bonding monomers N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - Deutsche Physikalische Gesellschaft (DPG)-Frühjahrtagung 2018 CY - Berlin, Germany DA - 11.03.2018 KW - Thermoresponsive polymer KW - UCST-type polymer KW - H bonds KW - Diaminopyridine KW - Acrylamide PY - 2018 AN - OPUS4-44569 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad A1 - Ahmadi, Vahid T1 - Upper critical solution temperature (UCST)-type thermoresponsive polymers from monomers with hydrogen-bonding interactions N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and/or 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - Invited Talk (Prof. Christine Papadakis) Technische Universität München - Soft Matter Physics CY - Munich, Germany DA - 03.07.2018 KW - Thermoresponsive polymer KW - UCST-type polymer KW - H bonds KW - Diaminopyridine KW - Acrylamide PY - 2018 AN - OPUS4-45423 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Controlled self-assembly of Janus dendrimers via microfluidics N2 - Vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) -5 as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of end groups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over self assembly/mixing and thus over size, morphology and size distribution of the vesicles. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous production of soft nanoparticles. Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process. T2 - Invited talk Leibniz Institute of Polymer Research Dresden (IPF) CY - Dresden, Germany DA - 08.03.2018 KW - Vesicles KW - Janus dendrimers KW - Microfluidics PY - 2018 AN - OPUS4-44441 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle T1 - Building macromolecular mimetics of cell constituents N2 - One of the holy grails in chemistry is to reconstitute some of life’s functions with or within synthetic materials. In this contribution, we demonstrate that “simple” macromolecular architectures such as dendritic amphiphiles, Janus dendrimers, thermoresponsive and hybrid organic-inorganic (co)polymers enable to mimic some of the functions of proteins for biomineralization, natural bactericides, biological membranes or the stimuli-responsive cytoskeleton. T2 - Chemiedozententagung 2018 CY - Jena, Germany DA - 05.03.2018 KW - UCST-type polymers KW - Bioinspiration KW - Thermoresponsive polymers PY - 2018 AN - OPUS4-44442 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Taabache, Soraya A1 - Bertin, Annabelle T1 - Dendritic Amphiphiles as Macromolecular Mimetics of Cellular Constituents N2 - One of the holy grails in chemistry is to reconstruct some of life’s functions within synthetic materials. In this contribution, we demonstrate that “simple” macromolecular architectures such as dendritic amphiphiles, Janus dendrimers, thermoresponsive and hybrid organic-inorganic (co)polymers enable to mimic some of the functions of proteins for biomineralization, natural bactericides, biological membranes or the stimuli-responsive cytoskeleton. T2 - Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS) - Dpt. des Matériaux Organiques (DMO), invited talk by Prof. Laurent Douce CY - Strasbourg, France DA - 09.02.2018 KW - Dendritic amphiphile KW - Antibacterial properties KW - Vesicles KW - Microfluidic PY - 2018 AN - OPUS4-44146 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, A. A1 - Ahmadi, V. T1 - Upper Critical Solution Temperature (UCST)-type Thermoresponsive Polymers from Hydrogen-Bonding Monomers N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications,but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or Ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and/or 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - Bordeaux Polymer Conference BPC 2018 CY - Bodeaux, France DA - 28.05.2018 KW - Acrylamide KW - Thermoresponsive polymer KW - UCST-type polymer KW - H-bonds KW - Diaminopyridine PY - 2018 AN - OPUS4-45155 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Kent, B. A1 - ten Brummelhuis, N. A1 - Schönhals, Andreas A1 - Asadujjaman, Asad T1 - Upper Critical Solution Temperature (UCST)-type thermoresponsive polymers from acrylamide-based monomers N2 - UCST-type thermoresponsive polymers that phase separate from solution upon cooling present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel UCST-type polymers because of their hydrophilic nature (with the right side chain) and propensity to form hydrogen bonds. We want to present our latest results on the copolymer poly(acrylamide-co-acrylonitrile) (P(AAm-co-AN)) that present a UCST in water as well as on two homopolymers based on an acrylamide derivative of 2,6-diaminopyridine, namely poly(N-(6-aminopyridin-2-yl)acrylamide) (PNAPAAm) and poly(N-(6-acetamidopyridin-2-yl)acrylamide) (PNAcAPAAm) that show UCST-type thermoresponsiveness in water/alcohol mixtures. Our focus for P(AAm-co-AN)) is its aggregation behaviour above and below its phase transition temperature as the size of thermoresponsive polymeric systems is of prime importance for biomedical applications (as size dependent processes take place in the body) and is linked to the optical properties of a material that matter in materials science. In the case of PNAPAAm and PNAcAPAAm, we focused on the co-solvency/co-non solvency effect on the phase transition temperature in water/alcohol mixture. Indeed, polymers with UCST behavior below 60°C in water/alcohol mixtures are extremely promising for the preparation of “smart” materials for sensing. T2 - Soft smart responsive materials workshop: Fundamentals and applications (SmartCECAM) CY - Mainz, Germany DA - 11.05.2017 KW - Thermoresponsive polymers KW - UCST-type polymers KW - poly(acrylamide-co-acrylonitrile) KW - 2,6-diaminopyridine-based polymers KW - co-solvency in water/acohol mixture PY - 2017 AN - OPUS4-40211 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad A1 - Ahmadi, Vahid A1 - Schönhals, Andreas A1 - ten Brummelhuis, N. T1 - Upper critical solution temperature (UCST)-type thermoresponsive polymers from hydrogen-bonding monomers N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - UCT&IOCB Theoretical Chemistry Seminars CY - University of Chemistry and Technology, Department of Physical Chemistry, Prague, Czech Republic DA - 24.11.2017 KW - Thermoresponsive polymers KW - UCST polymers KW - 2,6-diaminopyridine PY - 2017 AN - OPUS4-43129 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Czarnecki, Sebastian A1 - Hackelbusch, Sebastian T1 - Bioinspired hybrid organic-inorganic copolymers N2 - The demand for high-performance materials has strongly increased over the last decade. One way to improve their performance is to introduce material gradients as found in Nature (for example squid beaks, spider fangs, mussel byssal threads). One path towards the achievement of such material gradients is the synthesis of hybrid (gradient) copolymers, for instance based on silane and organic monomers. Since not all gradient copolymers can be synthesized by utilising the reactivity ratios of the monomers, forced gradients have to be used. However, in order to obtain gradient copolymers at high conversions, living or pseudo-living copolymerizations have to be performed and so far only few hybrid (organic / inorganic) gradient copolymers have been reported. In this contribution we will present the synthesis of a novel organic / inorganic hybrid copolymer via controlled radical polymerization. T2 - 5th International Conference on Multifunctional, Hybrid and Nanomaterials CY - Lisbon, Portugal DA - 06.03.2017 KW - Hybrid organic-inorganic copolymers KW - RAFT polymerization KW - ATRP polymerization PY - 2017 AN - OPUS4-39464 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Schönhals, Andreas A1 - ten Brummelhuis, N. A1 - Ahmadi, Vahid A1 - Asadujjaman, Asad T1 - Upper critical solution temperature (UCST)-type thermoresponsive polymers from acrylamide-based monomers N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the right side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - Bioorganik 2017 – 26th Symposium "Bioorganic Chemistry" for young researchers CY - Berlin, Germany DA - 20.09.2017 KW - Thermoresponsive polymers KW - UCST polymers KW - 2,6-diaminopyridine KW - Acrylamide PY - 2017 AN - OPUS4-42007 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Taabache, Soraya A1 - Maskos, M. T1 - Controlled Self-Assembly of Janus Dendrimers via Microfluidics N2 - Unilamellar vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of endgroups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis. Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process. T2 - 10th International Dendrimer Symposium CY - Weihai, China DA - 05.08.2017 KW - Micromixers KW - Janus dendrimers KW - Vesicles KW - Self-assembly PY - 2017 AN - OPUS4-41464 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad A1 - Ahmadi, Vahid T1 - Upper critical solution temperature (UCST)-type thermoresponsive polymers from hydrogen-bonding monomers N2 - UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding. T2 - Séminaire Laboratoire de Chimie des Polymères (LCP), UPMC, Paris CY - Paris, France DA - 28.09.2017 KW - UCST-type polymers KW - H-bonding monomers PY - 2017 AN - OPUS4-42478 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Taabache, Soraya A1 - Maskos, M. T1 - Controlled self-assembly of Janus dendrimers via microfluidics N2 - Vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) -5 as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of end groups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis. Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process. T2 - 11th Young Scientists' Workshop, Fraunhofer ICT-IMM CY - Mainz, Germany DA - 27.09.2017 KW - Vesicles KW - Dendrimersomes KW - Micromixer PY - 2017 AN - OPUS4-42479 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Taabache, Soraya A1 - Maskos, M. T1 - Controlled self-assembly of Janus dendrimers via microfluidics N2 - Vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of end groups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis. Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process. T2 - 6th Annual workshop on biomaterials and their interactions with biological and model membranes 2017 CY - Altafulla, Spain DA - 07.09.2017 KW - Janus dendrimers KW - Dendrimersomes KW - Microfluidic PY - 2017 AN - OPUS4-41903 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Barnefske, Lena A1 - Wachtendorf, Volker T1 - Self-healing silicone rubber for fluorescent partial discharge POF sensors in high-voltage cable accessories N2 - To avoid a catastrophic failure of insulation in high-voltage (HV) applications, a monitoring of partial discharges (PDs) is necessary. Fluorescently labelled polymer optical fibers (F-POF) offer an electrically passive method for PD detection in HV facilities. F-POFs could be embedded in HV cable accessories, which are usually made of silicone rubber. Herein they detect the light emitted by the PD and convert it into an electrical signal that can be monitored. Due to the difficult accessibility of HV cable accessories, a self-healing silicone rubber with prolonged service life after PD detection represents an attractive material design for HV accessories. With this contribution, we would like to present and discuss the possibilities of combining self-healing materials with POF-based sensors for PD detection in HV applications. T2 - 26th International Conference on Plastic Optical Fibres CY - Aveiro, Portugal DA - 13.09.2017 KW - Fluorescent polymer optical fibres KW - Partial discharge detection KW - High voltage cable accessories KW - Self-healing KW - Silicone rubber PY - 2017 SN - 978-989-97345-2-4 SP - paper 16, 1 EP - 5 AN - OPUS4-42510 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Barnefske, Lena T1 - Entwicklung eines mechanisch verstärken und selbstheilenden Silikonelastomers auf Basis eines Kapsel-basierten Ansatzes N2 - Im Arbeitskreis von Herrn Prof. Dr. Menzel (TU Braunschweig) wurde in Sievershausen ein Vortrag zum Thema „Self-healing and mechanically reinforced silicone rubber by the use of multifuctional capsules“ gehalten. Der Vortrag beginnt mit einer kurzen Motivation und einem Überblick über selbstheilende Materialien. Daraufhin werden die Ergebnisse zur Entwicklung eines selbstheilenden Silikonelastomers auf Basis von Kapseln, bestehend aus einem PDMS Kern und einer POS Hülle, dargestellt. Es folgt die Analytik, die auf DLS, TGA, UV/Vis und Fluoreszenzspektroskopie sowie SEM beruht. Der Vortrag endet mit einem Ausblick über zukünftige Arbeiten auf dem Gebiet. T2 - Seminar in Sievershausen CY - Sievershausen, Lehrte, Germany DA - 07.06.2017 KW - Selbstheilung KW - PDMS PY - 2017 AN - OPUS4-40857 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Barnefske, Lena A1 - Wachtendorf, Volker T1 - Self-healing silicone rubber for F-POF partial discharge sensors in HV cable accessories N2 - To avoid a catastrophic failure of insulation in high-voltage (HV) applications, a monitoring of partial discharges (PD) is necessary. Fluorescently labelled polymer optical fibres (F-POF) offer an electrically passive method for PD detection in HV facilities. F-POF could be embedded into HV cable insulation material, which are usually made of silicone rubber. Due to the difficult accessibility of HV cable accessories, a self-healing silicone rubber, based on incorporated capsules, with prolonged service life after PD detection represents an attractive material design for HV electrical insulation. T2 - 26th International Conference on Plastic Optical Fibres CY - Aveiro, Portugal DA - 13.09.2017 KW - Fluorescent polymer optical fibres KW - Partial discharge detection KW - High voltage cable accessories KW - Self-healing KW - Silicone rubber PY - 2017 AN - OPUS4-42511 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Auer, C. A1 - Kalinka, Gerhard A1 - Krause, T. A1 - Hinrichsen, G. T1 - Crystallization Kinetics of Pure and Fiber-Reinforced Poly(phenylene Sulfide) KW - Verbundwerkstoffe KW - Thermoplaste KW - Kristallisation KW - Kristallisationskinetik KW - Erstarrung KW - Avrami KW - Modellrechnung KW - Simulation PY - 1994 SN - 0021-8995 SN - 1097-4628 VL - 51 SP - 407 EP - 413 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-11991 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Rockland, Ulrike T1 - Jahresbericht 2009 T1 - Annual report 2009 T3 - BAM Reports/Jahresberichte - 2009 PY - 2010 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4546 SN - 0934-9456 N1 - Volltext (PDF) in deutsch und englisch - Full text (PDF) in German and English VL - 2009 SP - 1 EP - 118 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-454 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Rockland, Ulrike T1 - Jahresbericht 2008 T1 - Annual report 2008 T3 - BAM Reports/Jahresberichte - 2008 PY - 2009 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4550 SN - 0934-9456 N1 - Volltext (PDF) in deutsch und englisch - Full text (PDF) in German and English VL - 2008 SP - 1 EP - 110 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-455 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Rockland, Ulrike T1 - Jahresbericht 2007 T1 - Annual report 2007 T3 - BAM Reports/Jahresberichte - 2007 PY - 2008 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4564 SN - 0934-9456 N1 - Volltext (PDF) in deutsch und englisch - Full text (PDF) in German and English VL - 2007 SP - 1 EP - 153 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-456 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Rockland, Ulrike T1 - Jahresbericht 2006 T1 - Annual report 2006 T3 - BAM Reports/Jahresberichte - 2006 PY - 2007 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4578 SN - 0934-9456 N1 - Volltext (PDF) in deutsch und englisch - Full text (PDF) in German and English VL - 2006 SP - 1 EP - 108 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-457 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Lexow, Jürgen T1 - Jahresbericht 2004 T1 - Annual report 2004 T3 - BAM Reports/Jahresberichte - 2004 PY - 2005 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4592 SN - 0934-9456 VL - 2004 SP - 1 EP - 97 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-459 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN T1 - Jahresbericht 2002 T3 - BAM Reports/Jahresberichte - 2002 PY - 2003 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4619 SN - 0934-9456 VL - 2002 SP - 1 EP - 282 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-461 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Rockland, Ulrike T1 - Jahresbericht 2013 T1 - Annual report 2013 T3 - BAM Reports/Jahresberichte - 2013 PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-4507 SN - 0934-9456 N1 - Volltext (PDF) in deutsch und englisch - Full text (PDF) in German and English VL - 2013 SP - 1 EP - 122 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-450 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 26, Heft 4 T3 - Amts- und Mitteilungsblatt der BAM - 4/1996 PY - 1996 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553300 SN - 0340-7551 VL - 26 IS - 4 SP - 663 EP - 1214 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55330 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 26, Heft 3 T3 - Amts- und Mitteilungsblatt der BAM - 3/1996 PY - 1996 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553316 SN - 0340-7551 VL - 26 IS - 3 SP - 339 EP - 666 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55331 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 26, Heft 2 T3 - Amts- und Mitteilungsblatt der BAM - 2/1996 PY - 1996 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553325 SN - 0340-7551 VL - 26 IS - 2 SP - 119 EP - 340 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55332 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 26, Heft 1 T3 - Amts- und Mitteilungsblatt der BAM - 1/1996 PY - 1996 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553339 SN - 0340-7551 VL - 26 IS - 1 SP - 1 EP - 120 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55333 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 25, Heft 4 T3 - Amts- und Mitteilungsblatt der BAM - 4/1995 PY - 1995 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553342 SN - 0340-7551 VL - 25 IS - 4 SP - 765 EP - 924 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55334 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 25, Heft 3 T3 - Amts- und Mitteilungsblatt der BAM - 3/1995 PY - 1995 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553369 SN - 0340-7551 VL - 25 IS - 3 SP - 629 EP - 768 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55336 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 28, Heft 2 T3 - Amts- und Mitteilungsblatt der BAM - 2/1998 PY - 1998 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553097 SN - 0340-7551 VL - 28 IS - 2 SP - 191 EP - 498 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55309 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 28, Heft 1 T3 - Amts- und Mitteilungsblatt der BAM - 1/1998 PY - 1998 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553106 SN - 0340-7551 VL - 28 IS - 1 SP - 1 EP - 194 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55310 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 27, Heft 4 T3 - Amts- und Mitteilungsblatt der BAM - 4/1997 PY - 1997 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553114 SN - 0340-7551 VL - 27 IS - 4 SP - 889 EP - 958 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55311 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 27, Heft 3 T3 - Amts- und Mitteilungsblatt der BAM - 3/1997 PY - 1997 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553127 SN - 0340-7551 VL - 27 IS - 3 SP - 635 EP - 892 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55312 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 27, Heft 2 T3 - Amts- und Mitteilungsblatt der BAM - 2/1997 PY - 1997 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553138 SN - 0340-7551 VL - 27 IS - 2 SP - 401 EP - 640 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55313 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 27, Heft 1 T3 - Amts- und Mitteilungsblatt der BAM - 1/1997 PY - 1997 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553145 SN - 0340-7551 VL - 27 IS - 1 SP - 1 EP - 404 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55314 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 25, Heft 2 T3 - Amts- und Mitteilungsblatt der BAM - 2/1995 PY - 1995 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553376 SN - 0340-7551 VL - 25 IS - 2 SP - 331 EP - 630 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55337 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR T1 - Amts- und Mitteilungsblatt, Band 25, Heft 1 T3 - Amts- und Mitteilungsblatt der BAM - 1/1995 PY - 1995 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-553393 SN - 0340-7551 VL - 25 IS - 1 SP - 1 EP - 336 PB - Wirtschaftsverlag NW CY - Bremerhaven AN - OPUS4-55339 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN ED - Panne, Ulrich T1 - BAM Report 2019 T1 - BAM report 2019 N2 - Dieser BAM-Report erscheint zwischen zwei historischen Jubiläen: dem 30. Jahrestag des Mauerfalls am 9. November 1989 und dem der staatlichen Einheit Deutschlands am 3. Oktober 1990. Für unser Land bedeuten beide Daten eine glückliche Zäsur. Und auch für die Bundesanstalt für Materialforschung und -prüfung (BAM), die in den Jahren der Teilung ihren Sitz im westlichen Teil Berlins behalten hatte, waren sie mit guten Veränderungen verbunden: Zur BAM sind über 500 Wissenschaftler*innen des ostdeutschen Amtes für Standardisierung, Messwesen und Warenprüfung sowie aus den Instituten der Akademie der Wissenschaften in Berlin-Adlershof dazugekommen. Die BAM hat damals neue Tätigkeitsschwerpunkte gewonnen, vor allem auf dem Gebiet der Analytischen Chemie, und konnte sich als Teil des sich auch heute noch rasant entwickelnden Wissenschaftsstandortes Berlin-Adlershof positionieren. Blicken wir heute auf die bewegten und bewegenden Monate vor 30 Jahren zurück, so tun wir dies aus einer deutlich veränderten Gegenwart: Aktuell beschäftigen uns große gesellschaftliche Herausforderungen wie die digitale Transformation, Energiesicherheit, demografische Veränderungen und der Klimawandel. Berlin ist inmitten dieser Herausforderungen ein Ort der Innovation und des Aufbruchs in der Mitte Europas. Dafür steht beispielhaft die Ansiedlung des Werner von Siemens Centre for Industry & Science, das in den kommenden Jahren im Nordwesten der Stadt wachsen wird. Die BAM ist auch hier Partner des Zukunftsprojekts. Sicherheit in Technik und Chemie zu gewährleisten - unser Kernauftrag bleibt inmitten dieses beschleunigten Wandels unverändert gültig. Aber er bezieht sich heute auf die Sicherheit von Nanopartikeln, von Werkstücken aus dem 3D-Drucker oder die Speicher von Wasserstoffautos und morgen auf ganz neue Technologien. Dazu forschen wir in unseren fünf Themenfeldern Energie, Infrastruktur, Umwelt, Material und Analytical Sciences weltweit vernetzt. Über alle Umbrüche hinweg leitet uns dabei eine Idee: Sicherheit macht Märkte. Technologischer Wandel, Kreativität und Erfinder*innengeist ermöglichen den Wohlstand unserer Gesellschaft. Zugleich aber gilt: Erst die Verlässlichkeit neuer Technologien und Materialien schafft das Vertrauen der Menschen in den Wandel und sichert so langfristig unsere Zukunft. N2 - This BAM Report will be published between two historical events: the 30th anniversary of the fall of the Berlin Wall on 9 November 1989 and the 30th anniversary of German unification on 3 October 1990. Not only were these two dates joyful turning-points for our country, they also brought about positive changes for the Bundesanstalt für Materialforschung und -prüfung (BAM), which kept its headquarters in the western part of Berlin during the years of division. More than 500 scientists from the East German Amt für Standardisierung, Messwesen und Warenprüfung (Office for Standardisation, Metrology and Product Testing) and from the institutes of the Academy of Sciences in Berlin Adlershof joined BAM. At that time BAM added new areas of activity, especially in the field of analytical chemistry, and was able to position itself as part of the still rapidly developing Berlin Adlershof science centre. If we look back today at the eventful and moving months 30 years ago, we do so from a vastly different present. We are currently dealing with major societal challenges such as digital transformation, energy security, demographic shifts and climate change. In the midst of these challenges, Berlin is a place of innovation and new beginnings at the heart of Europe. This is exemplified by the Werner von Siemens Centre for Industry & Science, which will grow in the northwest of the city in the coming years. Ensuring safety in technology and chemistry remains our core mission amid this accelerated change. While today we focus on the safety of nanoparticles, components made by 3D printers or storage devices for hydrogen cars, tomorrow we will tackle other new technologies. To this end, we are conducting research in our five focus areas of energy, infrastructure, environment, materials and analytical sciences with partners worldwide. One idea guides us through all these changes: safety creates markets. Technological developments, creativity and innovation make the prosperity of our society possible. However, it is the reliability of new technologies and materials that creates trust in change and thus secures our future long-term. T3 - BAM Reports/Jahresberichte - 2019 PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-506376 SN - 0934-9456 SN - 2627-0153 SN - 2940-7532 N1 - Volltext (PDF) in deutsch und englisch - Full text (PDF) in German and English. VL - 2019 SP - 1 EP - 122 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-50637 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -