TY - JOUR A1 - Traulsen, C. H.-H. A1 - Kunz, V. A1 - Heinrich, Thomas A1 - Richter, S. A1 - Holzweber, Markus A1 - Schulz, A. A1 - von Krbek, L. K. S. A1 - Scheuschner, U. T. J. A1 - Poppenberg, J. A1 - Unger, Wolfgang A1 - Schalley, C. A. T1 - Synthesis and coordinative layer-by-layer deposition of pyridine-functionalized gold nanoparticles and tetralactam macrocycles on silicon substrates N2 - Coordination chemistry was applied to deposit pyridine-functionalized gold nanoparticles on silicon substrates. The particles were synthesized through the Brust/Schiffrin route with a subsequent ligand exchange reaction yielding well-defined particles of two different sizes. Multilayer deposition was carried out on a pyridine-terminated SAM, anchored on a hydroxyl-terminated silicon surface. Analogously, Hunter/Vögtle-type tetralactam macrocycle multilayers were deposited as well as mixed layers containing both either in an alternating sequence or as a macrocycle multilayer with a terminating nanoparticle layer. These composite layers were examined with respect to their ability to bind squaraine axles in the macrocycle cavities. The amount of guest bound is higher for the composite layer with alternating macrocycles and nanoparticles. KW - Layer-by-layer deposition KW - Functionalized Au nanoparticles KW - SEM KW - TEM KW - DLS KW - XPS KW - NEXAFS KW - ToF-SIMS KW - IR KW - UV-vis PY - 2013 DO - https://doi.org/10.1021/la403222x SN - 0743-7463 SN - 1520-5827 VL - 29 IS - 46 SP - 14284 EP - 14292 PB - American Chemical Society CY - Washington, DC AN - OPUS4-29699 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 - Bayerl, C. A1 - Shahryari, M. A1 - Reiter, R. A1 - Proß, V. A1 - Lehmann, K. A1 - Kühl, A. A. A1 - Becker, Dorit A1 - Schulz, Andreas A1 - Infante Duarte, C. A1 - Taupitz, M. A1 - Geisel, D. A1 - Tzschätzsch, H. A1 - Saatz, Jessica A1 - Traub, Heike A1 - Asbach, P. T1 - Quantitative Analysis of Gadolinium Deposits in Liver Tissue of Patients After Single or Multiple Gadolinium-based Contrast Agent Application N2 - Gadolinium-based contrast agents (GBCAs) are widely used in magnetic resonance imaging. Concerns exist regarding gadolinium deposition and its potential histopathologic tissue alterations, especially after repeated administrations of linear, less stable GBCAs. This study aimed to quantify gadolinium mass fractions in liver specimens of subjects exposed to GBCAs in correlation with histopathologic features. In this study, mass fractions of gadolinium in human liver specimens from 25 subjects who underwent liver tumor resection surgery and had received GBCA (1 to 9 times over 4 years), were quantitatively analyzed using inductively coupled plasma–mass spectrometry (ICP-MS). Histomorphology was assessed based on the nonalcoholic fatty liver disease activity score (NAS). Our results suggest that after intravenous administration of GBCA, a small fraction of gadolinium is retained in the liver over a time period of at least several weeks. A relationship was observed between Gadolinium retention and the number of GBCA administrations, but not with the cumulative dose and the degree of fatty liver disease. KW - ICP-MS KW - Contrast agent KW - Gadolinium KW - Liver PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-646608 DO - https://doi.org/10.1097/RLI.0000000000001254 SN - 1536-0210 SP - 1 EP - 10 PB - Lippincott Williams & Wilkins CY - Philadelphia, Pa. AN - OPUS4-64660 LA - eng 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 - Kosslick, H. A1 - Pitsch, I. A1 - Deutsch, J. A1 - Pohl, M.-M. A1 - Schulz, A. A1 - Vu, A.T. A1 - Nguyen, D.T. A1 - Frunza, L. A1 - Jäger, Christian T1 - Improved large mesoporous ordered molecular sieves - Stabilization and acid/base functionalization N2 - The preparation of nanoporous materials with enhanced stability using an improved synthesis route using reactive inorganic silica and alumina species is reported. This way improved mesoporous molecular sieves were obtained. The synthesized aluminum substituted mesoporous molecular materials (Al-MMS) contain very large pores of 50–200 Å size combined with an improved pore wall thickness. Increased wall thickness and Al substitution lead to an improved chemical stability against alkaline solution. The textural, structural and acid properties are investigated by physico-chemical methods. The catalytic performance acidic materials was tested in the benzoylation reaction; amino functionalized materials were studied in the base catalyzed Michael addition. KW - Nanoporous molecular sieve KW - Al substitution KW - Stability KW - Synthesis KW - Acidity KW - Catalysis PY - 2010 DO - https://doi.org/10.1016/j.cattod.2010.03.005 SN - 0920-5861 VL - 152 IS - 1-4 SP - 54 EP - 60 PB - Elsevier CY - Amsterdam AN - OPUS4-23960 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz-Forberg, Bernd A1 - Ulrich, A. T1 - Transport of RAM in Tanks - How to fit into the IAEA safety philosophy T2 - 7th International symposium Packaging and Transportation of Radioactive Materials CY - New Orleans, La., USA DA - 15.05.1983 PY - 1983 VL - 1 SP - 54 EP - 58 AN - OPUS4-36464 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 - JOUR A1 - Prasetiadi, A. E. A1 - Jost, M. A1 - Schulz, Baerbel A1 - Quibeldey, M. A1 - Rabe, Torsten A1 - Follmann, R. A1 - Jakoby, R. T1 - Liquid-crystal-based amplitude tuner and tunable SIW filter fabricated in LTCC technology N2 - Tunable microwave devices will play an important role in future wireless systems, in which high-frequency bands, e.g. millimeter waves, will become promising, due to its huge spectrum availability. At such frequency bands, liquid crystals (LCs) exhibit low microwave loss, which is excellent compared with the other tuning elements. In this paper, LC-based microwave components are fabricated by using low temperature co-fired ceramic technology, allowing the integration of the LC into microwave structures. The first component, the Amplitude tuner, controls the signal’s amplitude by using the interference concept, which exhibits a tunable attenuation range from 11 dB to 30 dB at 30 GHz. The second component is a 3-pole tunable bandpass filter, which is realized by using a substrate integrated waveguide topology, enabling a device with comparatively high-quality factors (Q-factors). The measurement results show Q-factors in the range of 68 to 100 for a frequency tuning of 29.4–30.1 GHz, i.e. a tuning range of 700 MHz, accompanied by an insertion loss 2 dB to 4 dB. KW - Passive components and circuits KW - Filters KW - Microwave technology PY - 2018 DO - https://doi.org/10.1017/S1759078718000600 SN - 1759-0787 VL - 10 IS - 5-6 SP - 674 EP - 681 PB - Cambridge University Press AN - OPUS4-46985 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Prasetiadi, A. E. A1 - Jost, M. A1 - Schulz, Bärbel A1 - Quibeldey, M. A1 - Rabe, Torsten A1 - Follmann, R. A1 - Jakoby, R. T1 - Liquid-Crystal-Based Amplitude Tuner Fabricated N2 - A 30GHz liquid-crystal-based amplitude tuner is proposed for the first time. The amplitude of a signal can be controlled by using the interference principle. An input signal is divided into a tunable liquid crystal phase shifter and a fixed transmission line. Later, the divided signals are combined together at the output port. The output amplitude depends on the phase difference between the tunable and the fixed line. The low temperature co-fired ceramic technology is utilized to fabricate the device. The measurement shows an attenuation range of 11 dB to 30 dB with a maximum biasing voltage of 100V. T2 - 12th European Microwave Integrated Circuits Conference CY - Nürnberg, Germany DA - 09.10.2017 KW - LTCC technology KW - Liquid crystals KW - RF components PY - 2017 SN - 978-2-87487-048-4 SN - 2325-0305 SP - 345 EP - 348 PB - IEEE AN - OPUS4-44752 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Eh Hovsepian, P. A1 - Ehiasarian, A. P. A1 - Purandare, Y. P. A1 - Mayr, P. A1 - Abstoss, K. G. A1 - Mosquera Feijoo, Maria A1 - Schulz, Wencke A1 - Kranzmann, Axel A1 - Lasanta, M. I. A1 - Trujillo, J. P. T1 - Novel HIPIMS deposited nanostructured CrN/NbN coatings for environmental protection of steam turbine components N2 - To increase efficiency, modern steam plants are pushing their operational regime from super-critical (600 °C/300 bar) to ultra-super-critical (740/760 °C/350 bar) stretching existing turbine materials to their limits. The focus is on new generation functional materials and technologies which complement the inherent properties of existing materials. Current work proposes a novel High Power Impulse Magnetron Sputtering (HIPIMS) Deposition technology, for the first time, for deposition of a ceramic based CrN/NbN coating with a nanoscale multilayer structure (bi-layer thickness Δ = 1.9 nm) with superior adhesion (LC2 = 80 N) to protect low Chromium P92 steel widely used in steam power plants. Thermodynamic calculations predict the equilibrium phases and aggressive gaseous compounds generated by the interaction of steam with the coating. CrN/NbN coated P92 steel samples oxidised at 600 °C in a high pressure (50 bar) 100% steam atmosphere for up to 1000 h reveal the coating's superior oxidation resistance and protective mechanisms, especially against the detrimental effect of Hydrogen. High temperature (650 °C) Tensile Strength, Low Cycle Fatigue and Creep tests confirm that, unlike other state-of-the-art PVD technologies, HIPIMS is not detrimental to the mechanical properties of the substrate material. Water droplet erosion tests confirm no measurable weight loss after 2.4 X 10⁶ impacts. KW - Hipims KW - CrN/NbN KW - Nanoscale multilayers KW - Steam oxidation resistance KW - Water droplet erosion resistance PY - 2018 DO - https://doi.org/10.1016/j.jallcom.2018.02.312 SN - 0925-8388 SN - 1873-4669 VL - 746 SP - 583 EP - 593 PB - Elsevier AN - OPUS4-44800 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nikfalazar, M. A1 - Kohler, C. A1 - Heunisch, Andreas A1 - Wiens, A. A1 - Zheng, Y. A1 - Schulz, Bärbel A1 - Mikolajek, M. A1 - Sohrabi, M. A1 - Rabe, Torsten A1 - Binder, R. A1 - Jakoby, R. T1 - LTCC phase shifters based on tunable ferroelectric composite thick films N2 - This paper presents, the investigation of tunable components based on LTCC technology, implementing ferroelectric tunable thick-film dielectric. The tunable loaded line phase shifters are fabricated with metal-insulator-metal (MIM) varactors to demonstrate the capabilities of this method for packaging of the tunable components. The MIM varactors consist of one tunable dielectric paste layer that is printed between two silver layers. The tunable ferroelectric paste is optimized for LTCC sintering temperature around 850°C. The phase shifters are fabricated in two different process. They were achieved a figure of merit of 24°/dB (phase shift 192°) at 3 GHz and 18°/dB (phase shift 98°) at 4.4 GHz by using seven unit cells that each unit cell consisting of two MIM varactors. KW - Ferroelectric KW - LTCC KW - Phase shifter KW - Fully printed component KW - BST PY - 2015 DO - https://doi.org/10.1515/freq-2015-0082 SN - 0016-1136 SN - 2191-6349 VL - 69 IS - 11-12 SP - 451 EP - 455 PB - De Gruyter CY - Berlin ; Boston, Mass. AN - OPUS4-34949 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz-Forberg, Bernd A1 - Zeisler, Peter A1 - Droste, Bernhard A1 - Kondratiev, A. A1 - Kozlov, J. A1 - Tichinov, N. T1 - Soviet-German cooperation in safety improvements of spent fuel transport casks N2 - The paper gives a survey of the Soviet (Russian) -German activities which started in 1988 with the objective of creating a long-term scientific-technical cooperation in the field of transport and storage casks for spent nuclear fuel. The first step, i.e., the step of informing each other about the state of development is done. The more complicated second phase with concerted common activities of both the Russian and German competent authorities and industrial enterprises is intended to start in the near future. T2 - PATRAM ´92 - 10th International symposium on the packaging and transportation of radioactive materials CY - Yokohama, Japan DA - 1992-09-13 PY - 1992 VL - 1 SP - 343 EP - 350 AN - OPUS4-21824 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pfennig, A. A1 - Linke, B. A1 - Schulz, Sabrina A1 - Kranzmann, Axel T1 - CO2-corrosion of steels exposed to saline water environment N2 - With CO2 being one reason for climate change carbon capture and storage (CCS) is discussed to mitigate climate change. When emission gases are compressed into deep geological layers CO2-corrosion can easily cause failure of injection pipes. Different steels 42CrMo4, X46Cr13 and X20Cr13 were tested as well as X35CrMo17 and X5CrNiCuNb16-4 in a laboratory Environment similar to the conditions of the CCS engineering site at the Northern German Bassin. Samples were exposed to synthetic aquifer water saturated with technical CO2 at a flow rate of 3 NL/h. Corrosion rates obtained via mass loss vary in a wide range (0,005 to 2.5 mm/year). The precipitations within the corrosion scale revealed a complicated multiphase layer containing siderite FeCO3, goethite α-FeOOH, lepidocrocite γ-FeOOH, mackinawite FeS and akaganeite Fe8O8(OH)8Cl1,34 and spinelphases of various compositions. T2 - TMS 2011 - 140th Annual Meeting & Exhibition CY - San Diego, CA, USA DA - 27.02.2011 KW - CCS KW - Steel KW - Corrosion KW - Carbon Capture and Storage PY - 2011 DO - https://doi.org/10.1002/9781118062173.ch102 VL - 3 IS - 0807 SP - 807 EP - 814 AN - OPUS4-23472 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bartoszek, M. A1 - Eckelt, R. A1 - Jäger, Christian A1 - Kosslick, H. A1 - Pawlik, Alf A1 - Schulz, A. T1 - Mesoporous silica-aluminas derived from precipitation: a study of the acidity, textural properties and catalytic performance KW - Silica-alumina KW - Solid state NMR KW - Acidity KW - Silicates KW - Tetrahedral aluminium PY - 2009 DO - https://doi.org/10.1007/s10853-009-3580-y SN - 0022-2461 SN - 1573-4803 VL - 44 IS - 24 SP - 6629 EP - 6636 PB - Springer Science + Business Media B.V. CY - Norwell, Mass. AN - OPUS4-20462 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Frunza, S. A1 - Schönhals, Andreas A1 - Frunza, L. A1 - Ganea, P. A1 - Kosslick, H. A1 - Harloff, J. A1 - Schulz, A. T1 - Molecular relaxation processes in a MOF-5 structure revealed by broadband dielectric spectroscopy: signature of phenylene ring fluctuations N2 - The molecular mobility of a MOF-5 metal–organic framework was investigated by broadband dielectric spectroscopy. Three relaxation processes were revealed. The temperature dependence of their relaxation rates follows an Arrhenius law. The process observed at lower temperatures is attributed to bending fluctuations of the edges of the cages involving the Zn–O clusters. The processes ('region II') at higher temperatures were assigned to fluctuations of phenyl rings in agreement with the NMR data found by Gould et al. (J. Am. Chem. Soc. 2008, 130, 3246). The carboxylate groups might also be involved. The rotational fluctuations of the phenyl rings leading to the low frequency part of relaxation region II might be hindered either by some solvent molecules entrapped in the cages or by an interpenetrated structure and have a broad distribution of activation energies. The high frequency part of region II corresponds nearly to a Debye-like process: This is explained by a well-defined structure of empty pores. PY - 2010 DO - https://doi.org/10.1021/jp1071617 SN - 1520-6106 SN - 1520-5207 SN - 1089-5647 VL - 114 IS - 40 SP - 12840 EP - 12846 PB - Soc. CY - Washington, DC AN - OPUS4-22255 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Marieta, C. A1 - Schulz, Eckhard A1 - Irusta, L. A1 - Gabilondo, N. A1 - Tercjak, A. A1 - Mondragon, I. T1 - Evaluation of fiber surface treatment and toughening of thermoset matrix on the interfacial behaviour of carbon fiber-reinforced cyanate matrix composites N2 - Composites of carbon fiber and cyanate ester matrix have been investigated. The research has been focused on the interfacial behaviour. The influence of carbon fiber surface treatments, sizing and oxidation, and also modification of thermoset matrix by the addition of a thermoplastic, has been analysed. In order to relate the interfacial behaviour with the characteristics of the components, a physico-chemical characterisation of the carbon fibers and of the cyanate ester resins has been carried out. Thereafter, the apparent interfacial shear strength, the interlaminar shear strength and the Mode II delamination fracture toughness, GIIC, have been measured by pull-out test, short beam-shear test, and end-notched flexure test, respectively. For fractographic analysis the surfaces of laminates fractured under Mode II deformation have also been examined by scanning electron microscopy. KW - Carbon fiber composites KW - Cyanate ester KW - Thermoplastic KW - Interfacial bonding KW - Mechanical properties KW - Morphology PY - 2005 DO - https://doi.org/10.1016/j.compscitech.2005.05.008 SN - 0266-3538 VL - 65 IS - 14 SP - 2189 EP - 2197 PB - Elsevier CY - Barking AN - OPUS4-10891 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz-Forberg, Bernd A1 - Lauer, A. T1 - ESP: Beurteilung elektronischer Fahrdynamiksysteme durch den ATT und Stand der internationalen Diskussion N2 - Untertitel: Zur Funktionsweise der Systeme Unterscheidung in Fahrzeug-Stabilisierung und Anhänger-Wank-Stabilisierungsfunktion Stand von Wissenschaft und Technik allgemein anerkannte Regeln der Technik Warum ist die Wirkvorschrift so wichtig? Gibt es Alternativen? Ist eine Einführung von elektronischen Fahrstabilisierungseinrichtungen auch ohne gesetzliche Vorgabe denkbar? Einbindung in den Markt (u. a. Bustouristik) Welche weiteren Vorstöße werden unternommen, um die vorhandenen Systeme in Regelwerke und damit in die Flotten einzuführen? Vorgehen in Dänemark T2 - anlässlich des Symposiums Aktuelle Entwicklungen im Gefahrgutrecht und der Fahrzeugkonstruktion im Rahmen der 60. IAA Nutzfahrzeuge CY - Hanover, Germany DA - 2004-09-30 PY - 2004 AN - OPUS4-4280 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hinrichs, V. A1 - Leistner, A. A1 - Kalinka, Gerhard A1 - Schulz, Eckhard A1 - Hinrichsen, G. T1 - Viscoelastic properties of the interphase in fibre reinforced polymers - measurement and simulation KW - Polymer KW - Glass fibre KW - Interphase KW - Coating KW - Glass transition KW - Dynamic KW - Viscoelastic PY - 1999 VL - 6 IS - 2 SP - 93 EP - 101 PB - North-Holland CY - New York, NY AN - OPUS4-12003 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Becker, Roland A1 - Reck, Günter A1 - Radeglia, Reiner A1 - Springer, A. A1 - Schulz, Burkhard T1 - Designed self-assembly of a bimolecular calix[4]resorcinarene capsule held together by hydrogen bonds N2 - The X-ray crystallographic study of the macrocyclic tetrakis-N[N-2-hydroxyethyl-piperazino]calix[4]resorcinarene·3CH3CH2OH·H2O (3) reveals a self-assembled dimeric capsule-like complex held together by an array of intermolecular hydrogen bonds. Pairs of concave molecules associate directly in bowl-to-bowl fashion and enclose an accessible supramolecular cavity of Å3 hosting one water and three ethanol molecules. The supramolecular arrangement displays alternating layers of facing bowls and interlocking lower rim aliphatic moieties. The helical conformation of the 2-hydroxyethyl piperazinomethyl moieties displays chirality of a bimolecular capsule frozen in the solid state. 3 crystallises in the triclinic space group P-1 with two symmetry independent molecules in the asymmetric unit. Two enantiomeric capsules form a racemic pair in the unit cell. KW - Hydrogen bonded molecular capsule KW - Conformational chirality KW - Calix[4]resorcinarenes KW - Crystal structure PY - 2006 DO - https://doi.org/10.1016/j.molstruc.2005.08.027 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 784 IS - 1-3 SP - 157 EP - 161 PB - Elsevier CY - Amsterdam AN - OPUS4-12241 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bismarck, A. A1 - Pfaffernoschke, M. A1 - Springer, J. A1 - Schulz, Eckhard T1 - Polystyrene-grafted Carbon Fibers: Surface Properties and Adhesion to Polystyrene N2 - It is highly desirable to improve attractive interactions between carbon fibers and unreactive thermoplastic matrices to the possible maximum. This could be achieved by a simple grafting process to create a covalently bonded interface or interlayer, which should result in cohesive interactions between the polymer-grafted fibers and the same matrix material, leading to a better adhesion strength in the obtained composite material. Here, we are describing the grafting of styrene onto unmodified and unsized carbon fibers via free-radical bulk polymerization in the presence of fibers. After grafting, the surface properties of the carbon fiber approach those of pure polystyrene which was proven by contact angle and zeta ({zeta}) potential measurements. As indicated by the water contact angle, the carbon fiber surface becomes more hydrophobic. Scanning electron microscopy (SEM) provides evidence of grafted polymer. This simple procedure results in a continuous polystyrene coating. The fiber diameter increases significantly after polymer grafting. The adhesion and fracture behavior between the original and polystyrene-grafted carbon fibers to a polystyrene (VESTYRON®) matrix was characterized using the single-fiber pull-out test. There is a considerable increase in the measurable adhesion, i.e., the interfacial shear strength IFSS, by almost 300% between the grafted fibers and polystyrene as compared to untreated original fibers. Two planes of interfacial failure could be distinguished; first in the fiber coating interface leading to lower interfacial shear strength and second in the PS-matrix-PS-coating interphase resulting in a higher interfacial shear strength. In addition to the improved adhesion, there are also clear differences in the pull-out behavior between the nongrafted and grafted fibers. After the initial debonding process corresponding to the maximal pull-out force is completed, the pull-out force is increasing again. PY - 2005 DO - https://doi.org/10.1177/0892705705049559 SN - 0892-7057 SN - 1530-7980 VL - 18 IS - 4 SP - 307 EP - 331 PB - Sage Publ. CY - London AN - OPUS4-11599 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ho, K.K.C. A1 - Lamoriniere, S. A1 - Kalinka, Gerhard A1 - Schulz, Eckhard A1 - Bismarck, A. T1 - Interfacial behavior between atmospheric-plasma-fluorinated carbon fibers and poly(vinylidene fluoride) N2 - Atmospheric-plasma fluorination was used to introduce fluorine functionalities onto the surface of carbon fibers without affecting their bulk properties. The interfacial adhesion between atmospheric-plasma-fluorinated carbon fibers and poly(vinylidene fluoride) (PVDF) was studied by means of direct wetting measurements and single fiber pullout tests. Measured contact angles of PVDF melt droplets on modified carbon fibers show that short exposure times of carbon fibers to atmospheric-plasma fluorination (corresponding to a degree of surface fluorination of F/C = 0.01 (1.1%)) leads to improved wettability of the fibers by PVDF melts. The apparent interfacial shear strength as a measure of practical adhesion, determined by the single-fiber pullout test, increases by 65% under optimal treatment conditions. The improved practical adhesion is not due to the formation of transcrystalline regions around the fibers or a change of the bulk matrix crystallinity or to an increased surface roughness; it seems to be due to the compatibilization of the interface caused of the atmospheric-plasma fluorination of the carbon fibers. KW - Carbon fibers KW - Fluorination KW - Contact angle KW - Interface KW - Adhesion KW - Surface area KW - Fiber properties PY - 2007 DO - https://doi.org/10.1016/j.jcis.2007.04.076 SN - 0021-9797 SN - 1095-7103 VL - 313 IS - 2 SP - 476 EP - 484 PB - Elsevier CY - Orlando, Fla. AN - OPUS4-16026 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schulz, Ulrich A1 - Jansen, Kirsten A1 - Braig, A. ED - Marosi, G. J. T1 - Light stabilizers under attack by acid rain T2 - 2nd International Conference on Modification, Degradation and Stabilization of Polymers ; 2nd MoDeSt CY - Budapest, Hungary DA - 2002-06-30 PY - 2002 SN - 3-527-30706-0 SN - 1022-1360 N1 - Serientitel: Macromolecular symposia – Series title: Macromolecular symposia IS - 202 SP - 1 PB - Wiley-VCH CY - Weinheim AN - OPUS4-1645 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schulz, Ulrich A1 - Jansen, Kirsten A1 - Braig, A. T1 - Stabilizers in Automotive Coatings under Acid Attack N2 - To examine the action of acid atmospheric precipitation on the light stabilisers in automotive coatings two common clearcoat types (TSA and 2K-PU) blended with commercially available HALS and UVA were subjected to artificial weathering (Acid Dew and Fog test and Acid-free weathering test) and natural weathering outdoors in Jacksonville, FL. Tracing gloss and haze during weathering the test results showed that the influence of acid stress on the long-term performance of the clearcoats depended on the kind of the stabilisation system. T2 - 26th FATIPEC Congress CY - Dresden, Germany DA - 2002-09-09 KW - Coatings KW - Ageing KW - Stabilisation KW - HALS KW - Gloss KW - Acid resistance PY - 2002 DO - https://doi.org/10.1002/1521-3900(200209)187:1<835::AID-MASY835>3.0.CO;2-Y SN - 1022-1360 SN - 0258-0322 SN - 1521-3900 VL - 187 SP - 835 EP - 844 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-1647 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Stock, H.-R. A1 - Schulz, A. A1 - Kopnarski, M. A1 - Gross, Thomas ED - Ricard, A. T1 - Standards for composition-depth profiles of TiN, Ti(C, N) and (Ti, Al)N with different chemical composition T2 - 5th International Conference on Plasma Surface Engineering (PSE) CY - Garmisch-Patenkirchen, Germany DA - 1996-09-09 KW - Beschichtung KW - Plasma PY - 1996 SN - 0257-8972 VL - 97 IS - 1-3 SP - 181 PB - Elsevier CY - Amsterdam AN - OPUS4-636 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Habib, Abdel Karim A1 - Bonow, G. A1 - Kroll, A. A1 - Hegenberg, J. A1 - Schmidt, L. A1 - Barz, T. A1 - Schulz, D. T1 - Forschungsprojekt RoboGasInspector: Gaslecksuche mit autonomen mobilen Robotern N2 - Im Rahmen des Förderprogramms AUTONOMIK des Bundesministeriums für Wirtschaft und Technologie wurde in einem Konsortium aus neun Projektpartnern der Prototyp eines autonomen mobilen Roboters zur Gaslecksuche in ausgedehnten Industrieanlagen entwickelt. Anhand verschiedenartiger Sensorik zur Selbstlokalisation und Navigation wurde die autonome Beweglichkeit des Systems für beliebige Anlagen realisiert, mit der Option anhand von Teleoperation manuell in den Prozess einzugreifen. Ausgestattet mit Video- und Gasfernmesstechnik ist der Roboter imstande, Inspektionsaufgaben in Industrieanlagen durchzuführen, ohne in mögliche Gefahrenbereiche direkt einfahren zu müssen und ohne, dass ein Mensch vor Ort anwesend ist. Der Roboter kann zur routinemäßigen Inspektion von Anlagen oder zur gezielten Untersuchung spezifischer Anlagenteile eingesetzt werden. Dank der verwendeten Fernmesstechnik können auch Anlagenteile inspiziert werden, die aufgrund ihrer beschränkten Zugänglichkeit mittels herkömmlicher Messtechnik nur schwer zu inspizieren sind. KW - Lecksuche KW - Roboter KW - Gasausbreitung KW - Simulation PY - 2013 SN - 2191-0073 VL - 3 IS - 5 SP - 10 EP - 15 PB - Springer-VDI-Verl. CY - Düsseldorf AN - OPUS4-29586 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kovalchuck, Anton V. A1 - Bricks, Julia A1 - Reck, Günter A1 - Rurack, Knut A1 - Schulz, Burkhard A1 - Szumna, A. A1 - Weißhoff, Hardy T1 - A charge transfer-type fluorescent molecular sensor that "lights up" in the visible upon hydrogen bond-assisted complexation of anions PY - 2004 DO - https://doi.org/10.1039/b405207b SN - 0022-4936 SN - 0009-241x SN - 1359-7345 SN - 1364-548x SP - 1946 EP - 1947 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-4123 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Weimann, Karin A1 - Matyschik, Jan A1 - Adam, Christian A1 - Schulz, T. A1 - Linß, E. A1 - Müller, A. T1 - Optimierung des Rückbaus/Abbruchs von Gebäuden zur Rückgewinnung und Aufbereitung von Baustoffen unter Schadstoffentfrachtung (insbes. Sulfat) des RCMaterials sowie ökobilanzieller Vergleich von Primär- und Sekundärrohstoffeinsatz inkl. Wiederverwertung N2 - Aufgrund der großen Massenströme ist das Recycling von Baurestmassen von besonderer Bedeutung für die Schonung von natürlichen Ressourcen. Eine wichtige Voraussetzung für ein hochwertiges Recycling, wie z.B. eine Wiederverwertung von aufbereitetem Bauschutt/Altbeton als rezyklierte Gesteinskörnung im Hochbau, ist die Einhaltung von Grenzwerten für Stör- und Schadstoffe. Dabei steht der Sulfatgehalt im Eluat von Bauschutt besonders im Fokus. In der vorliegenden Studie wird untersucht, wie durch die Optimierung von Abbrucharbeiten und Bauschuttaufbereitung hochwertige Gesteinskörnungen aus Altbeton gewonnen werden können. Anhand von Literatur- und Datenrecherchen werden zunächst Sulfatquellen in Gebäuden sowie verfügbare Abbruch- und Aufbereitungstechniken zusammengestellt. Am Beispiel von unterschiedlichen Gebäudetypen werden Szenarien für selektiven und nicht selektiven Abbruch (Schwerpunkt: Sulfatentfachtung) in Hinblick auf ihre Umweltwirkungen ökobilanziell bewertet. Ergänzt werden diese Bewertungen durch Untersuchungen an realen Bauschuttmaterialien und Abbruchprojekten. Auf dieser Basis werden Handlungsempfehlungen für die Gewinnung von hochwertigen RC-Gesteinskörnungen erarbeitet und diskutiert.----------------------------------------------------------------------------------------- Due to the large-scale mass flow of construction and demolition wastes, the recycling of those residues is of particular importance for the conservation of natural resources. An important requirement for recycling on a high level, like the reuse of crushed concrete as recycled concrete aggregate, is the observation of limits for hazardous substances and impurities. This study is focusing on the reduction of sulphates in the eluate of crushed concrete. An investigation of possibilities to optimize demolition and dismantling as well as treatment of crushed concrete with the objective of gaining recycled concrete aggregates of high quality. Based on a literature research and a data review the origins of sulfates in buildings and also the availability of techniques for demolition and treatment of crushed concrete are listed and evaluated. Using the examples of different building types scenarios for selective dismantling and non-selective demolition (focused on reducing suphates) are evaluated in terms of affecting the environment. In addition samples from real demolition construction sites and plants for treatment of construction rubble were investigated. Based on these results recommendations for the production of high quality recycled concrete aggregates are worked out. KW - Bauschuttaufbereitung KW - Abbruch KW - Ökobilanzielle Bewertung KW - RC-Beton KW - Gips KW - Abbruchverfahren KW - Hochwertiges Recycling KW - Ökobilanzielle Betrachtung KW - Sulfatentfachtung KW - Demolition/dismantling KW - Treatment of C&D wastes KW - High-grade recycling KW - Environmental LCA KW - Reduction of sulphates PY - 2012 UR - http://www.umweltbundesamt.de/publikationen/optimierung-des-rueckbausabbaus-von-gebaeuden-zur SN - 1862-4804 SP - 1 EP - 227 PB - Umweltbundesamt CY - Dessau-Roßlau AN - OPUS4-26999 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hartmann, S. A1 - Shaporin, A. A1 - Hermann, S. A1 - Bonitz, J. A1 - Heggen, M. A1 - Meszmer, P. A1 - Sturm, Heinz A1 - Hölck, O. A1 - Blaudeck, T. A1 - Schulz, S. E. A1 - Mehner, J. A1 - Gessner, T. A1 - Wunderle, B. T1 - Towards nanoreliability of CNT-based sensor applications: Investigations of CNT-metal interfaces combining molecular dynamics simulations, advanced in situ experiments and analytics N2 - In this paper we present results of our recent efforts to understand the mechanical interface behaviour of single-walled carbon nanotubes (CNTs) embedded in metal matrices. We conducted experimental pull-out tests of CNTs embedded in Pd or Au and found Maximum forces in the range 10 - 102 nN. These values are in good agreement with forces obtained from molecular Dynamics simulations taking into account surface functional Groups (SFGs) covalently linked to the CNT material. The dominant failure mode in experiment is a CNT rupture, which can be explained with the presence of SFGs. To qualify the existence of SFGs on our used CNT material, we pursue investigations by means of fluorescence labeling of surface species in combination with Raman imaging. We also report of a tensile test system to perform pull-out tests inside a transmission electron microscope to obtain in situ images of CNT-metal interfaces under mechanical loads at the atomic scale. T2 - 2015 16th International Conference on Thermal, Mechanical and Multi-Physics Simulation and Experiments in Microelectronics and Microsystems CY - Budapest, Hungary DA - 20.4.2015 KW - Carbon nanotube CNT KW - Metal matrix KW - Pull-out test KW - Molecular dynamics simulation KW - Surface functional groups KW - Fluorescence labeling KW - Raman imaging KW - Tensile test inside a TEM PY - 2015 SN - 978-1-4799-9950-7 VL - 2015 SP - 1 EP - 8 PB - IEEE AN - OPUS4-37625 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Weimann, Karin A1 - Müller, A. A1 - Linß, E. A1 - Schulz, T. A1 - Adamczyk, Burkart ED - Jones, M.R. ED - Newlands, M.D. ED - Halliday, J.E. ED - Csetenyi, L.J. ED - Li, Z. ED - McCarthy, M.J. ED - Dyer, T.D. T1 - Reducing sulphates in crushed concrete: improving the building material properties of recycled concrete aggregates N2 - The material properties of recycled concrete aggregates (RCA) are correlated to the sorting accuracy of the former demolition waste. Impurities like wood, clay bricks or gypsum can lead to inferior building material properties. Harmful substances like heavy metals or organic pollutants should be minimised as well. Hence the non-concrete materials have to be separated from the concrete material stream. This can be done during the demolition process by using selective dismantling techniques. Alternatively a variety sorting and classifying techniques to purify the crushed concrete can be utilized. A research project, funded by the Federal Ministry for the Environment, Nature Conservation and Nuclear Safety, investigated the possibilities of gaining recycled concrete aggregates of a high quality for the reuse in the production of concrete. The work focuses especially on how gypsum respectively sulphates in the crushed concrete can be reduced. Sulphates can impair the setting behaviour of concrete and also damage set concrete by causing expansion. Therefore the content of sulphates in RCA is restricted by guidelines and standards in Germany. Generally, gypsum in construction waste originates from interior fittings like gypsum walls, floor screeds, plaster boards and also plaster. Most of these materials can be reconstructed using selective dismantling techniques. This can be achieved either by manual labour or by using mechanical equipment e.g. to remove floor screeds by milling. Depending on the specific deconstruction site it can be more effective and/or more environmentally compatible to remove sulphates by treating the crushed concrete. Applicable treatments for sulphate reduction include dry processes like manual sorting of gypsum wall blocks as well as wet treatments e.g. jigging. In addition this research project an environmental performance evaluation was undertaken to assess different techniques for reducing sulphates in recycled concrete aggregates. T2 - Tagung 'Cocrete in the low carbon era' CY - Dundee, Great Britain DA - 09.07.2012 KW - Building material properties KW - Environmental performance evaluation KW - Gypsum KW - Recycled concrete aggregates KW - Sulphates PY - 2012 SN - 978-0-9573263-0-9 SP - 687 EP - 698 AN - OPUS4-26211 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Prasetiadi, A .E. A1 - Jost, M. A1 - Schulz, Bärbel A1 - Quibelday, M. A1 - Rabe, Torsten A1 - Follmann, R. A1 - Jakoby, R. T1 - Liquid-Crystal-Based Amplitude Tuner Fabricated N2 - 30GHz liquid-crystal-based amplitude tuner is proposed for the first time. The amplitude of a signal can be controlled by using the interference principle. An input Signal is divided into a tunable liquid crystal phase shifter and a fixed transmission line. Later, the divided signals are combined together at the output port. The output amplitude depends on the phase difference between the tunable and the fixed line. The low temperature co-fired ceramic technology is utilized to fabricate the device. The measurement shows an attenuation range of 11 dB to 30 dB with a maximum biasing voltage of 100V. T2 - 47th European Microwave Conference CY - Nürnberg, Germany DA - 10.10.2017 KW - LTCC technology KW - Liquid crystals KW - RF components PY - 2017 SN - 978-2-87487-047-7 SN - 2325-0305 SP - 1085 EP - 1088 PB - IEEE AN - OPUS4-44753 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 -