TY - CONF A1 - Lüth, Peter A1 - Brandes, E. A1 - Frost, K. A1 - Kurth, Lutz A1 - Schmidt, Martin A1 - Michael-Schulz, Heike A1 - Uhlig, S. T1 - CEQAT-DGHS Ringversuchsprogramm der BAM in Kooperation mit QuoData und PTB N2 - Bei der Bewertung der Verlässlichkeit der im Labor gewonnenen Prüfergebnisse spielen Ringversuche eine entscheidende Rolle. Die Bundesanstalt für Materialforschung und -prüfung (BAM) unterstützt deshalb den weiteren Ausbau des Ringversuchsprogramms des im Jahr 2007 gegründeten Kompetenzzentrums zur Qualitätssicherung für Prüfungen von Gefahrgütern und Gefahrstoffen auf physikalische Gefahren (Centre for quality assurance for testing of dangerous goods and hazardous substances, CEQAT-DGHS). Bei allen bisher untersuchten Prüfmethoden besteht ein Verbesserungsbedarf. Die RV müssen daher zunächst auf die Methodenentwicklung, -verbesserung und -validierung abzielen und nicht auf Leistungstests. T2 - 14. Kolloquium zur chemischen und physikalischen Sicherheitstechnik (BAM-PTB-Kolloquium) CY - Berlin, Germany DA - 14.06.2016 KW - Gefahrgut KW - Gefahrstoff KW - Ringversuch KW - Prüfmethode KW - Validierung KW - Qualitätssicherung PY - 2016 SN - 978-3-9817853-5-7 SN - 0938-5533 SP - 143 EP - 143 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-38464 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lüth, Peter A1 - Brandes, E. A1 - Frost, K. A1 - Kurth, Lutz A1 - Schmidt, Martin A1 - Michael-Schulz, Heike A1 - Uhlig, S. T1 - CEQAT-DGHS Ringversuchsprogramm für die Chemikaliensicherheit -Methodenvalidierung N2 - Bei der Bewertung der Verlässlichkeit der im Labor gewonnenen Prüfergebnisse spielen Ringversuche eine entscheidende Rolle. Die Bundesanstalt für Materialforschung und –prüfung (BAM) unterstützt deshalb den weiteren Ausbau des Ringversuchsprogramms des im Jahr 2007 gegründeten Kompetenzzentrums zur Qualitätssicherung für Prüfungen von Gefahrgütern und Gefahrstoffen auf physikalische Gefahren (Centre for quality assurance for testing of dangerous goods and hazardous substances, CEQAT-DGHS). Bei allen bisher untersuchten Prüfmethoden besteht ein Verbesserungsbedarf. Die RV müssen daher zunächst auf die Methodenentwicklung, -verbesserung und -validierung und auf die Bestimmung der Messunsicherheit der jeweiligen Prüfmethode abzielen und nicht auf Leistungstests. T2 - Behörden-Erfahungsaustausch CY - Berlin, Germany DA - 4. Juni 2018 KW - Prüfmethode KW - Methodenvalidierung KW - Gefahrgut KW - Gefahrstoff KW - Qualitätssicherung PY - 2018 AN - OPUS4-45297 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schulz, T. A1 - Reimann, T. A1 - Bochmann, A. A1 - Vogel, A. A1 - Capraro, B. A1 - Mieller, Björn A1 - Teichert, S. A1 - Töpfer, J. T1 - Sintering behavior, microstructure and thermoelectric properties of calcium cobaltite thickfilms for transversal thermoelectric multilayer generators N2 - The sintering behavior and the thermoelectric performance of Ca3Co4O9 multilayer laminates were studied, and a multilayer thermoelectric generator was fabricated. Compacts and multilayer samples with anisotropic microstructure and residual porosity were obtained after conventional sintering at 920 °C, whereas dense and isotropic multilayer samples were prepared by firing at 1200 °C and reoxidation at 900 °C. A hot-pressed sample has a dense and anisotropic microstructure. Samples sintered at 920 °C exhibit low electrical conductivity due to the low density, whereas the Seebeck coefficient is not sensitive to preparation conditions. However, thermal conductivity of multilayers is very low, and, hence acceptable ZT values are obtained. A ransversal multilayer thermoelectric generator (TMLTEG) was fabricated by stacking layers of Ca3Co4O9 green tapes, AgPd conductor printing, and co-firing at 920 °C. The TMLTEG has a power output of 3 mW at ΔT =200 K in the temperature interval of 25 °C to 300 °C. KW - Thermoelectric oxide KW - Calcium cobaltite KW - Pressure-assisted sintering KW - Multilayer PY - 2018 DO - https://doi.org/10.1016/j.jeurceramsoc.2017.11.017 SN - 0955-2219 SN - 1873-619X VL - 38 IS - 4 SP - 1600 EP - 1607 PB - Elsevier Ltd. AN - OPUS4-43983 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Jost, M. A1 - Strunck, S. A1 - Heunisch, Andreas A1 - Wiens, A. A1 - Prasetiadi, A.E. A1 - Weickhmann, C. A1 - Schulz, Bärbel A1 - Quibeldey, M. A1 - Karabey, O.H. A1 - Rabe, Torsten A1 - Follmann, R. A1 - Koether, D. A1 - Jakoby, R. T1 - Continuously tuneable liquid crystal based stripline phase shifter realised in LTCC technology N2 - This work presents the design, fabrication and measurements of a low temperature cofired ceramic (LTCC) integrated liquid crystal (LC) phase shifter. The effective permittivity of the phase shifter and therefore its differential phase shift can be tuned continuously by orienting the LC directors with electric fields. The phase-shift demonstrator is designed for Ka-band frequencies around 30 GHz and represents a stripline filled with LC, embedded inside an LTCC multilayer structure, which provides a space-qualified and hermetically-sealed LC cavity within an RF-capable material system. The total length of the device is 37 mm while the phase shifting LC section has a length of 14.6 mm. At 30 GHz it exhibits a differential phase shift of 60° with an insertion loss around 6 dB, resulting in a figure of merit around 10°/dB. An advantage is that the insertion loss is nearly independent of the tuning state of the LC. The response time of the phase shifter, depending on the desired LC orientation, is between 62 ms and 37 s. T2 - EuMC 2015 - 45th European microwave conference CY - Paris, France DA - 07.09.2015 PY - 2015 SN - 978-2-87487-039-2 SP - 1260 EP - 1263 AN - OPUS4-35268 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Strunck, S. A1 - Gaebler, A. A1 - Karabey, O.H. A1 - Heunisch, Andreas A1 - Schulz, Bärbel A1 - Rabe, Torsten A1 - Follmann, R. A1 - Kassner, J. A1 - Koether, D. A1 - Manabe, A. A1 - Jakoby, R. T1 - Reliability study of a tunable ka-band SIW-phase shifter based on liquid crystal in LTCC-technology N2 - A tunable substrate-integrated waveguide phase shifter using low-temperature co-fired ceramic (LTCC)-technology is presented in this paper. By changing the effective permittivity in the liquid crystal (LC)-filled waveguide, the differential phase can be tuned continuously. This is achieved by means of an analog signal applied to the electrodes, surrounding the LC. The design allows for precise tuning of the differential phase, which is proven with a Monte Carlo measurement resulting in phase errors of less than 3° at 28 GHz. Besides that, the ambient temperature dependency of the module is shown. The phase shifter has a high integration level and can be included into a complete and lightweight single-phased array antenna module. The phase shifter is realized with a high level of integration which is available through the multilayer process of the LTCC. It has a length of 50 and provides a differential phase shift of more than 360° at 28 GHz. The figure of merit for tunable phase shifters is >40°/dB. KW - Passive components and circuits KW - New and emerging technologies and materials PY - 2014 DO - https://doi.org/10.1017/S175907871400083X SN - 1759-0787 SN - 1759-0795 SP - 1 EP - 7 PB - Cambridge Univ. Press CY - Cambridge AN - OPUS4-31198 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Knelles, J. A1 - Wanner, C. A1 - Schulz, F. A1 - Freund, M. A1 - Kolmangadi, Mohamed Aejaz A1 - Baro, A. A1 - Huber, P. A1 - Schönhals, Andreas A1 - Lachat, S. T1 - Liquid crystalline hydrazones revisited: dipolar interactions vs hydrogen bonding affecting mesomorphic properties N2 - In order to understand the role of dipolar interactions vs. H-bonding, a series of hydrazones were synthesised from 4-alkoxy-, 3,4-dialkoxy- or 3,4,5-trialkoxybenzaldehydes and phenyl, bromo- or nitrophenylhydrazine, respectively. Their mesomorphic properties were investigated by differential scanning calorimetry (DSC), polarising optical microscopy (POM), X-ray diffraction (WAXS, SAXS) and compared with known members. Only those hydrazones derived from 3,4,5-trisalkoxybenzaldehyde and either meta, meta-dinitro- or ortho, para-dinitrophenylhydrazine displayed hexagonal columnar mesophases. All other derivatives were non-mesomorphic, even when H-bonds were present. Dipole moments of the various nitro-substituted hydrazones were experimentally determined by dielectric measurements and supported by theoretical DFT calculations, which indicated that the mesophase formation is mostly governed by strong dipole moment and further enforced by intramolecular H-bonding. KW - Discotic liquid crystals PY - 2021 DO - https://doi.org/10.1080/02678292.2021.1873438 VL - 48 IS - 10 SP - 1382 EP - 1391 PB - Taylor & Francis AN - OPUS4-52409 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lüth, Peter A1 - Brandes, E. A1 - Frost, K. A1 - Kurth, Lutz A1 - Schmidt, Martin A1 - Michael-Schulz, Heike A1 - Uhlig, S. T1 - CEQAT-DGHS Ringversuchsprogramm für die Chemikaliensicherheit – Methodenvalidierung N2 - Bei der Bewertung der Verlässlichkeit der im Labor gewonnenen Prüfergebnisse spielen Ringversuche eine entscheidende Rolle. Die Bundesanstalt für Materialforschung und –prüfung (BAM) unterstützt deshalb den weiteren Ausbau des Ringversuchsprogramms des im Jahr 2007 gegründeten Kompetenzzentrums zur Qualitätssicherung für Prüfungen von Gefahrgütern und Gefahrstoffen auf physikalische Gefahren (Centre for quality assurance for testing of dangerous goods and hazardous substances, CEQAT-DGHS). Bei allen bisher untersuchten Prüfmethoden besteht ein Verbesserungsbedarf. Die RV müssen daher zunächst auf die Methodenentwicklung, -verbesserung und -validierung und auf die Bestimmung der Messunsicherheit der jeweiligen Prüfmethode abzielen und nicht auf Leistungstests. T2 - 13. Fachtagung Anlagen-, Arbeits- und Umweltsicherheit CY - Köthen, Germany DA - 16.11.2017 KW - Gefahrgut KW - Gefahrstoff KW - Ringversuch KW - Prüfmethode KW - Validierung KW - Qualitätssicherung PY - 2017 SN - 978-3-96057-032-5 SP - 1 EP - 13 CY - Köthen AN - OPUS4-43299 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Malow, Marcus A1 - Michael-Schulz, Heike A1 - Salg, S. A1 - Schomäcker, R. T1 - Der Einfluss hohen Umgebungsdrucks auf Deflagrationen N2 - Das Deflagrationsverhalten von Feststoffen unter atmosphärischen Bedingungen wurde in der Vergangenheit eingehend untersucht. Standardmäßig wird die Deflagrationsprüfung in einem offenen System durchgeführt. Aber auch in geschlossenen Systemen ist die Deflagrationsprüfung durchführbar und sie liefert Ergebnisse, die mit den Standardmethoden vergleichbar sind. Darüber hinaus bietet die Prüfung in einem geschlossenen System den Vorteil, nicht nur die Temperatur, sondern auch den Druck messen und für die Beschreibung des Deflagrationsverlaufs heranziehen zu können. Auch für die Prüfung in geschlossenen Systemen liegt eine Reihe an experimentellen Ergebnissen vor. Von Klais wurde veröffentlicht, dass die Deflagrationsgeschwindigkeit, beschrieben anhand der Druckanstiegsrate, mit steigendem Druck ansteigt. Vor dem Hintergrund dieser experimentellen Beobachtung wurde interpretiert, dass die Steigerung der Geschwindigkeit ihre Ursache im steigenden Umgebungsdruck findet. Es wurde weiter versucht, einen funktionalen Zusammenhang zwischen Umgebungsdruck und Deflagrationsgeschwindigkeit, ausgedrückt durch die Druckanstiegsrate, herzustellen. Dabei wurde nicht beachtet, dass neben dem Umgebungsdruck noch andere Einflussfaktoren auf die Deflagrationsgeschwindigkeit gegeben sind. Wesentlich ist hierbei die für die Reaktion zur Verfügung stehende Oberfläche, die sich bei einer lokalen, punktförmigen Anzündung mit fortschreitender Reaktionszeit vergrößert. In diesem Beitrag wird der Einfluss des Umgebungsdrucks auf die Deflagrationsgeschwindigkeit systematisch untersucht. Zu diesem Zweck wurden Experimente bei verschiedenen Ausgangsdrücken bis zu 50 bar (abs) durchgeführt. Der Anfangsdruck, also der Druck der vor Beginn eines Experiments im Reaktionsraum herrscht, wurde schrittweise von einem Experiment zum nächsten erhöht. Für die Versuchsreihen wurden zwei Substanzen verwendet: Azodicarbonamid und ein Imidazolderivat. Diese unterscheiden sich in ihrem Deflagrationsverhalten und hinsichtlich der Gasmengenentwicklung. Die durchgeführten Experimente haben gezeigt, dass die Deflagrationsgeschwindigkeit mit steigendem Druck zunimmt. Sowohl die Druckanstiegsrate, als auch die lineare Ausbreitungsrate sind ein gutes Maß dafür. Zwischen den beiden Kenngrößen besteht ein linearer Zusammenhang. Für eine gegebene Geometrie lässt sich die eine Kenngröße aus der anderen berechnen. T2 - 5. Brand- und Explosionsschutztage 2017 CY - Magdeburg, Germany DA - 23.03.2017 KW - Deflagrationen KW - Geschlossenes System KW - Azodicarbonamid KW - Druckanstiegsrate KW - Deflagrationsgeschwindigkeit PY - 2017 SN - 978-3-00-056201-3 SP - 1 EP - 11 AN - OPUS4-39920 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kang, Y. A1 - Nack, L. M. A1 - Liu, Y. A1 - Qi, B. A1 - Huang, Y. A1 - Liu, Z. A1 - Chakraborty, I. A1 - Schulz, F. A1 - Ahmed, A. A. A. A1 - Poveda, M. C. A1 - Hafizi, F. A1 - Roy, S. A1 - Mutas, M. A1 - Holzapfel, M. A1 - Sanchez-Cano, C. A1 - Wegner, Karl David A1 - Feliu, N. A1 - Parak, W. J. T1 - Quantitative considerations about the size dependence of cellular entry and excretion of colloidal nanoparticles for different cell types N2 - Most studies about the interaction of nanoparticles (NPs) with cells have focused on how the physicochemical properties of NPs will influence their uptake by cells. However, much less is known about their potential excretion from cells. However, to control and manipulate the number of NPs in a cell, both cellular uptake and excretion must be studied quantitatively. Monitoring the intracellular and extracellular amount of NPs over time (after residual noninternalized NPs have been removed) enables one to disentangle the influences of cell proliferation and exocytosis, the major pathways for the reduction of NPs per cell. Proliferation depends on the type of cells, while exocytosis depends in addition on properties of the NPs, such as their size. Examples are given herein on the role of these two different processes for different cells and NPs. KW - Cell proliferation KW - Exocytosis KW - Gold nanoparticles KW - Quantum dots KW - Fluorescence KW - Uptake studies PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-543476 DO - https://doi.org/10.1007/s40828-021-00159-6 SN - 2199-3793 VL - 8 IS - 1 SP - 1 EP - 8 PB - Springer CY - Berlin AN - OPUS4-54347 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kang, Y. A1 - Nack, L. A1 - Liu, Y. A1 - Qi, B. A1 - Huang, Y. A1 - Liu, Z. A1 - Chakraborty, I. A1 - Schulz, F. A1 - Ahmed, A. A. A1 - Poveda, M. C. A1 - Hafizi, F. A1 - Roy, S. A1 - Mutas, M. A1 - Holzapfel, M. A1 - Sanchez-Cano, C. A1 - Wegner, Karl David A1 - Feliu, N. A1 - Parak, W. J. T1 - Correction to: Quantitative considerations about the size dependency for cellular entry and excretion of colloidal nanoparticles for different cell types N2 - We regret to inform that the labels "NPs which remain in endosomes/lysosomes" and "exocytosed NPs" had been erroneously swapped in the sketch on the right side in Figure 2. The corrected Fig. 2 is displayed below. WJP apologizes for this error. KW - Cell proliferation KW - Exocytosis KW - Gold nanoparticles KW - Quantum dots KW - Uptake studies PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-554519 DO - https://doi.org/10.1007/s40828-022-00168-z VL - 8 IS - 17 SP - 1 EP - 2 PB - Springer CY - Berlin AN - OPUS4-55451 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hartmann, S A1 - Sturm, Heinz A1 - Blaudeck, T A1 - Hoelck, O A1 - Hermann, S A1 - Schulz, SE A1 - Wunderle, B. T1 - Experimental and computational studies on the role of surface functional groups in the mechanical behavior of interfaces between single-walled carbon nanotubes and metals N2 - To study the mechanical interface behavior of single-walled carbon nanotubes (CNTs) embedded in a noble metal, we performed CNT-metal pull-out tests with in situ scanning electron microscope experiments. Molecular dynamics (MD) simulations were conducted to predict force-displacement data during pull-out, providing critical forces for failure of the system. In MD simulations, we focused on the influence of carboxylic surface functional groups (SFGs) covalently linked to the CNT. Experimentally obtained maximum forces between 10 and 102 nN in palladium and gold matrices and simulated achievable pulling forces agree very well. The dominant failure mode in the experiment is CNT rupture, although several pull-out failures were also observed. We explain the huge scatter of experimental values with varying embedding length and SFG surface density. From simulation, we found that SFGs act as small anchors in the metal matrix and significantly enhance the maximum forces. This interface reinforcement can lead to tensile stresses sufficiently high to initiate CNT rupture. To qualify the existence of carboxylic SFGs on our CNT material, we performed analytical investigation by means of fluorescence labeling of surface species and discuss the results. With this contribution, we focus on a synergy between computational and experimental approaches involving MD simulations, nano scale testing, and analytics (1) to predict to a good degree of accuracy maximum pull-out forces of single-walled CNTs embedded in a noble metal matrix and (2) to provide valuable input to understand the underlying mechanisms of failure with focus on SFGs. This is of fundamental interest for the design of future mechanical sensors incorporating piezoresistive single-walled CNTs as the sensing element. KW - Oxygen-containing functionalities KW - Molecular-dynamics KW - Structural characterization KW - Reinforced composites KW - Raman spectroscopy KW - Shear strength KW - Polymer matrix KW - Pull-out KW - Simulation KW - Purification PY - 2016 DO - https://doi.org/10.1007/s10853-015-9142-6 SN - 0022-2461 SN - 1573-4803 VL - 51 IS - 3 SP - 1217 EP - 1233 AN - OPUS4-35795 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Flores, E. A1 - Idrees, F. A1 - Moussay, P. A1 - Viallon, J. A1 - Wielgosz, R. A1 - Fernández, T. A1 - Ramírez, S. A1 - Rojo, A. A1 - Shinji, U. A1 - Waldén, J. A1 - Sega, M. A1 - Sang-Hyub, O. A1 - Macé, T. A1 - Couret, C. A1 - Qiao, H. A1 - Smeulders, D. A1 - Guenther, F.R. A1 - Thorn, W.J. III A1 - Tshilongo, J. A1 - Ntsasa, N.G. A1 - Stovcík, V. A1 - Valková, M. A1 - Konopelko, L. A1 - Gromova, E. A1 - Nieuwenkamp, G. A1 - Wessel, R. M. A1 - Milton, M. A1 - Harling, A. A1 - Vargha, G. A1 - Tuma, Dirk A1 - Kohl, Anka A1 - Schulz, Gert T1 - Final report on international comparison CCQM-K74: Nitrogen dioxide, 10 µmol/mol N2 - There is a high international priority attached to activities which reduce NOx in the atmosphere. The current level of permitted emissions is typically between 50 µmol/mol and 100 µmol/mol, but lower values are expected in the future. Currently, ambient air quality monitoring regulations also require the measurement of NOx mole fractions as low as 0.2 µmol/mol. The production of accurate standards at these levels of mole fractions requires either dilution of a stable higher concentration gas standard or production by a dynamic technique, for example one based on permeation tubes. The CCQM-K74 key comparison was designed to evaluate the level of comparability of National Metrology Institutes' measurement capabilities and standards for nitrogen dioxide (NO2) at a nominal mole fraction of 10 µmol/mol. The measurements of this key comparison took place from June 2009 to May 2010. Seventeen laboratories took part in this comparison coordinated by the BIPM and VSL. The key comparison reference value was based on BIPM measurement results, and the standard measurement uncertainty of the reference value was 0.042 µmol/mol. This key comparison demonstrated that the results of the majority of the participants agreed within limits of ±3% relative to the reference value. The results of only one laboratory lay significantly outside these limits. Likewise this comparison made clear that a full interpretation of the results of the comparison needed to take into account the presence of nitric acid (in the range 100 nmol/mol to 350 nmol/mol) in the cylinders circulated as part of the comparison, as well as the possible presence of nitric acid in the primary standards used by participating laboratories. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA). DatesIssue 1A (Technical Supplement 2012) KW - Ringversuch KW - NO2 KW - Spurenverunreinigungen KW - Meßverfahren PY - 2012 DO - https://doi.org/10.1088/0026-1394/49/1A/08005 SN - 0026-1394 SN - 1681-7575 VL - 49 IS - 08005 SP - 1 EP - 117 PB - Inst. of Physics Publ. CY - Bristol AN - OPUS4-25927 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Giebler, Rainer A1 - Unger, Wolfgang A1 - Schulz, B. A1 - Reiche, J. A1 - Brehmer, L. A1 - Wühn, M. A1 - Wöll, Ch. A1 - Smith, A.P. A1 - Urquhart, S.G. T1 - Near-Edge X-ray Absorption Fine Structure Spectroscopy on Ordered Films of an Amphiphilic Derivate of 2,5-Diphenyl-1,3,4-Oxadiazole KW - NEXAFS KW - OMBD KW - X-ray Absorption Spectroscopy PY - 1999 SN - 0743-7463 SN - 1520-5827 VL - 15 IS - 4 SP - 1291 EP - 1298 PB - American Chemical Society CY - Washington, DC AN - OPUS4-828 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bismarck, A. A1 - Lee, A.F. A1 - Sarac, A.S. A1 - Schulz, Eckhard A1 - Wilson, K. T1 - Electrocoating of carbon fibres: A route for interface control in carbon fibre reinforced poly methylmethacrylate? N2 - A simple method of creating defined PMMA and poly (MMA-co-Cz) electrocoatings on carbon fibres is described. The electrodeposition of poly methylmethacrylate (PMMA) onto unsized, unmodified carbon fibres was performed by simple constant current electrolyses of methylmethacrylate (MMA) monomer in dimethylformamide (DMF) solutions and the ‘pure’ liquid monomer using sodium nitrate and lithium perchlorate as supporting electrolytes. The presence of polymeric coatings successfully attached to the carbon fibres was verified by scanning electron microscopy and photoelectron spectroscopy (XPS). Performing the electrolysis in dilute MMA in DMF solutions ([MMA] < 5 M) results in the deposition of powder-like polymer on the carbon fibre electrodes. Increasing the MMA concentration in the DMF solution results in a homogeneous PMMA coating of the carbon fibres. The degree of grafting or coating increases with increasing MMA concentration, except when pure MMA is used without solvent. The adhesive strength between the electrocoated carbon fibres and a PMMA matrix was determined using the single fibre pull-out test. It was found that the interfacial fracture behaviour of all carbon fibre/PMMA model composites is rather brittle. The adhesion strength between the unmodified carbon fibres and the PMMA matrix was equal to the cohesive strength of the polymer matrix itself. Nevertheless, the electrodeposition of thin and homogeneous PMMA coatings resulted in much improved adhesion strengths. KW - Carbon fibres KW - Coating KW - Interfacial strength KW - Fibre - matrix bond KW - Photoelectron spectroscopy (XPS) PY - 2005 DO - https://doi.org/10.1016/j.compscitech.2005.01.006 SN - 0266-3538 VL - 65 IS - 10 SP - 1564 EP - 1573 PB - Elsevier CY - Barking AN - OPUS4-7540 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -