TY - JOUR A1 - Kipphardt, Heinrich A1 - Matschat, Ralf A1 - Vogl, Jochen A1 - Gusarova, Tamara A1 - Czerwensky, Michael A1 - Heinrich, Hans-Joachim A1 - Hioki, A. A1 - Konopelko, L.A. A1 - Methven, B. A1 - Miura, T. A1 - Petersen, O. A1 - Riebe, Gundel A1 - Sturgeon, R. A1 - Turk, G.C. A1 - Yu, L. L. T1 - Purity determination as needed for the realisation of primary standards for elemental determination: status of international comparability N2 - Within the National Metrology Institutes (NMIs) and designated laboratories, an interlaboratory comparison, CCQM-P107, was conducted to verify the degree of international comparability concerning the results of purity analysis. The mass fractions of Ag, Bi, Cd, Cr, Ni, Tl at the lower mg/kg-level in a high purity zinc material were determined, but the real measurand in metrological sense was the sum of the six mass fractions. Homogeneity was investigated by glow discharge mass spectrometry, reference values were obtained using isotope dilution mass spectrometry. Six NMIs participated, contributing eight independent data sets. The agreement amongst the results of the participants, their median and the agreement with the reference values were usually excellent and in almost all cases below the target uncertainty of 30% relative. In this manner, the accuracy of results and the comparability between the participants was demonstrated to be established. KW - Interlaboratory comparison KW - Purity analysis KW - High purity metals KW - CCQM-P107 KW - Zinc PY - 2010 DO - https://doi.org/10.1007/s00769-009-0557-0 SN - 0949-1775 SN - 1432-0517 VL - 15 IS - 1 SP - 29 EP - 37 PB - Springer CY - Berlin AN - OPUS4-20767 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - van der Hout, J. W. A1 - van der Veen, A. M. H. A1 - Ziel, P. R. A1 - Kipphardt, Heinrich A1 - Tuma, Dirk A1 - Maiwald, Michael A1 - Fernández, T. E. A1 - Gómez, C. A1 - Cieciora, D. A1 - Ochman, G. A1 - Dias, F. A1 - Silvino, V. A1 - Macé, T. A1 - Sutour, C. A1 - Marioni, F. A1 - Ackermann, A. A1 - Niederhauser, B. A1 - Fükő, J. A1 - Büki, T. A1 - Szilágyi, Z. N. A1 - Tarhan, T. A1 - Engin, E. T1 - International Comparison Euramet.QM-K111 – Propane in Nitrogen N2 - This key comparison aims to assess the core capabilities of the participants in gas analysis. Such competences include, among others, the capabilities to prepare Primary Standard gas Mixtures (PSMs), perform the necessary purity analysis on the materials used in the gas mixture preparation, the verification of the composition of newly prepared PSMs against existing ones, and the capability of calibrating the composition of a gas mixture. According to the Strategy for Key Comparisons of the Gas Analysis Working Group, this key comparison is classified as an RMO track A key comparison. The artefacts were binary mixtures of propane in nitrogen at a nominal amount-of-substance fraction level of 1000 μmol/mol. The values and uncertainties from the gravimetric gas mixture preparation were used as key comparison reference values (KCRVs). Each transfer standard had its own KCRV. The results are generally good. All results are within ± 1 % of the KCRV. KW - EURAMET.QM-K111 KW - Propane in nitrogen PY - 2017 DO - https://doi.org/10.1088/0026-1394/54/1A/08020 SN - 0026-1394 VL - 54 IS - Technical Supplement SP - 08020, 1 EP - 34 PB - IOP Science AN - OPUS4-44471 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - van der Veen, A. M H A1 - Zalewska, E. T. A1 - Kipphardt, Heinrich A1 - Beelen, R. R. A1 - Tuma, Dirk A1 - Maiwald, Michael A1 - Fükő, J. A1 - Büki, T. A1 - Szilágyi, Z. N. A1 - Beránek, J. A1 - Cieciora, D. A1 - Ochman, G. A1 - e.t al., T1 - Metrologia International Bureau of Weights and Measures (BIPM), find out more - KEY COMPARISON International comparison CCQM-K118 natural gas N2 - CCQM-K118 was an international key comparison on natural gas composition with two types of gases, i.e., a low calorific hydrogen-enriched natural gas and a high calorific LNG type of gas. There were 14 participating laboratories. The traveling standards (i.e., 14 mixtures each) were obtained from an external source and checked for homogeneity and stability before and after the participants' measurements at the two coordinating laboratories. The data evaluation was performed using a consensus value and a laboratory effect model. The results of the participants were benchmarked against a key comparison reference value computed from the largest consistent subset (LCS) of the submitted results, adjusted for the differences between the travelling standards. For the first time in a key comparison in gas analysis, the model included a term to account for excess variability in the LCS. Most of the participants reported one or a few (slightly) discrepant results. Partly this is due to the heterogeneity and heteroscedasticity of the datasets. In all, the results in this key comparison demonstrate the good comparability of the national measurement standards for natural gas composition maintained by the participating NMIs. 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). 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 https://www.bipm.org/kcdb/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA). KW - CCQM-K PY - 2022 DO - https://doi.org/10.1088/0026-1394/59/1A/08017 SN - 0026-1394 VL - 59 IS - 1A PB - IOP Publishing LTD AN - OPUS4-56308 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zhou, Z. A1 - Han, Q. A1 - Wang, D. A1 - Macé, T. A1 - Kipphardt, Heinrich A1 - Maiwald, Michael A1 - Tuma, Dirk A1 - Uehara, S. A1 - Akima, D. A1 - Shimosaka, T. A1 - Jung, J. A1 - Oh, S.-H. A1 - van der Veen, A. A1 - van Wijk, J.I.T. A1 - Ziel, P. R. A1 - Konopelko, L. A1 - Valkova, M. A1 - Mogale, D.M. A1 - Botha, A. A1 - Brewer, P. A1 - Murugan, A. A1 - Minnaro, M.D. A1 - Miller, M. A1 - Guenther, F. A1 - Kelly, M.E. T1 - CCQM K101 Final report international comparison CCQM-K101:Oxygen in nitrogen-a track B comparison and that the matrix contains argon N2 - This key comparison aims to assess the capabilities of the participants to determine the amount-of-substance fraction oxygen in nitrogen. The GAWG has classified this as a track B comparison, due to the unexpected 50 μmol/mol argon mole fraction content of the transfer standards, which effects the achievable performance of some measurement techniques such a GC-TCD. The separation of oxygen and argon is challenging, and not all systems in use are equally well designed for it. As this analytical challenge due to a substantial fraction of argon in the transfer standards became a reality, the Gas Analysis Working Group (GAWG) decided to qualify this key comparison as a regular key comparison and not as a core comparison, which may be used to support calibration and measurement capabilities (CMCs) for oxygen in nitrogen, or for oxygen in nitrogen mixtures containing argon only (see also the section on support to CMCs). KW - CCQM-K101 KW - Gas analysis PY - 2016 UR - http://iopscience.iop.org/article/10.1088/0026-1394/53/1A/08013 SN - 1681-7575 SN - 0026-1394 VL - 53 IS - Techn Suppl SP - 08013, 1 EP - 71 PB - IOP publishing AN - OPUS4-40013 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Kipphardt, Heinrich A1 - del Rocío Arvizu Torres, M. A1 - Manzano, J.V.L. A1 - Rodrigues, J.M. A1 - de Sena, R.C. A1 - Yim, Y.-H. A1 - Heo, S.W. A1 - Zhou, T. A1 - Turk, G.C. A1 - Winchester, M. A1 - Yu, L. L. A1 - Miura, T. A1 - Methven, B. A1 - Sturgeon, R. A1 - Jährling, R. A1 - Rienitz, O. A1 - Tunc, M. A1 - Can, S.Z. T1 - Final report of the key comparison CCQM-K72: Purity of zinc with respect to six defined metallic analytes N2 - KEY COMPARISON High purity elements can serve as a realization of the SI unit amount of substance for the specific element. Solutions prepared from high purity metals by applying gravimetric preparation and the concept of molar mass are used as 'calibration' solutions in many fields of analytical chemistry and provide the metrological basis in elemental analysis. Since ideal purity does not exist for real materials, the actual purity of the high purity material must be known with a specified uncertainty. As required uncertainties around 10-4 relative on the purity statement are not accessible in almost all cases by a direct measurement of the element in itself, the indirect approach is followed, where all elements excepting the matrix element itself are measured and their sum is subtracted from the value for ideal purity, which is 1 kg/kg. It was the aim of this comparison to demonstrate the capability of national metrology institutes and designated institutes to determine the purity of pure elements. In order to limit the effort within this comparison, only six metallic impurities (Ag, Al, Cd, Cr, Ni, Tl) in the low mg/kg range are considered in a zinc matrix. It has to be underlined here that the task was to measure the purity of zinc based on the determination of six analytes. The task is not trace analysis of specific analytes in zinc. This subtle distinction defines different measurands. The sample, pure Zn, was cut in pieces of cubic geometry for wet chemical analysis or of pin geometry for GDMS analysis and was sent to the participants. The comparison was run under the auspices of the Inorganic analysis Working Group (IAWG) of the CCQM and was piloted by the BAM Federal Institute for Materials Research and Testing, Berlin, Germany. The majority of the participants applied ICP-MS techniques and only two participants used additionally atomic absorption spectrometry. GDMS was used only by one participant. The observed spreads for the measurement results reported by the participants were significantly lower than those of the preceding study CCQM-P107 and were well below the target uncertainty of 30% relative. As a consequence, comparability within the participating laboratories is demonstrated to be established. The individual measurement results, mean values and medians derived were in all cases very consistent with the reference values obtained by IDMS and so the accuracy of the measurement results for the participating laboratories is as well demonstrated to be established. Especially with the results of CCQM-P62 and CCQM-P107 in mind, the outcome of CCQM-K72 can be considered as a big step forward in the community. CCQM is aware of the difference between a characterization based on only six analytes and a complete characterization. Therefore, the pilot study CCQM-P149 has been initiated and already started, which focuses on the fit-for-purpose approaches for the purity determination of metals (here: zinc) to be used as primary standards in elemental analysis. Another follow-up in the form of a pilot study on non-metal impurities is mandatory, because non-metal impurities such as oxygen, nitrogen and sulfur often make up the largest contributions. 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 (CIPM MRA). KW - CCQM KW - Metrology KW - Purity PY - 2014 DO - https://doi.org/10.1088/0026-1394/51/1A/08008 SN - 0026-1394 SN - 1681-7575 VL - 51 IS - 1A (Tech.Suppl. 2014) SP - 08008, 1 EP - 40 PB - Inst. of Physics Publ. CY - Bristol AN - OPUS4-30772 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Danilewsky, A.N. A1 - Rack, A. A1 - Wittge, J. A1 - Weitkamp, T. A1 - Simon, R. A1 - Riesemeier, Heinrich A1 - Baumbach, T. T1 - White beam synchrotron topography using a high resolution digital X-ray imaging detector N2 - X-ray topography is a well known imaging technique to characterise strain and extended defects in single crystals. Topographs are typically collected on X-ray films. On the one hand such photographic films show a limited dynamic range and the production of films will be discontinued step by step in the near future. On the other hand new imaging detectors improved for X-ray tomography become more and more attractive even for topography because of increasing resolution, dynamic range, speed and active area. In this paper we report about the upgrade of the TOPO–TOMO beamline at the synchrotron light source ANKA, Research Centre Karlsruhe, with a high resolution digital camera for the topography use. KW - White beam topography KW - Synchrotron radiation KW - Digital X-ray detector KW - Scintillator KW - Synchrotron instrumentation KW - Digital radiography PY - 2008 DO - https://doi.org/10.1016/j.nimb.2008.02.065 SN - 0168-583X SN - 1872-9584 VL - 266 IS - 9 SP - 2035 EP - 2040 PB - Elsevier CY - Amsterdam AN - OPUS4-18567 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rack, A. A1 - Weitkamp, T. A1 - Zanette, I. A1 - Morawe, C. A1 - Vivo Rommeveaux, A. A1 - Tafforeau, P. A1 - Cloetens, P. A1 - Ziegler, E. A1 - Rack, T. A1 - Cecilia, A. A1 - Vagovic, P. A1 - Harmann, E. A1 - Dietsch, R. A1 - Riesemeier, Heinrich T1 - Coherence preservation and beam flatness of a single-bounce multilayer monochromator (beamline ID19-ESRF) N2 - Larger spectral bandwidth and higher photon flux density are the major advantages of multilayer monochromators over crystal-based devices. Especially for synchrotron-based hard X-ray microimaging applications the increased photon flux density is important in order to achieve high contrast and resolution in space and/or time. However, the modifications on the beam profile induced by reflection on a multilayer are a drawback which can seriously harm the performance of such a monochromator. A recent study [A. Rack, T. Weitkamp, M. Riotte, D. Grigoriev, T. Rack, L. Helfen, T. Baumbach, R. Dietsch, T. Holz, M. Krämer, F. Siewert, M. Meduna, P. Cloetens, E. Ziegler, J. Synchrotron Radiat. 17 (2010) 496–510] has shown that the modifications in terms of beam flatness and coherence preservation can be influenced via the material composition of the multilayer coating. The present article extends this knowledge by studying further material compositions used on a daily basis for hard X-ray monochromatization at the beamline ID19 of the European Synchrotron Radiation Facility. KW - Multilayer mirrors KW - X-rays KW - X-ray optics KW - Coherence KW - X-ray monochromators KW - X-ray imaging KW - X-ray phase contrast KW - Synchrotron radiation PY - 2011 DO - https://doi.org/10.1016/j.nima.2010.11.069 SN - 0168-9002 SN - 0167-5087 VL - 649 IS - 1 SP - 123 EP - 127 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-25240 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vogl, Jochen A1 - Kipphardt, Heinrich A1 - Richter, Silke A1 - Bremser, Wolfram A1 - Arvizu Torres, M. A1 - Lara Manzano, J. A1 - Buzoianu, M. A1 - Hill, S. A1 - Petrov, P. A1 - Goenaga-Infante, H. A1 - Sargent, M. A1 - Fisicaro, P. A1 - Labarraque, G. A1 - Zhou, T. A1 - Turk, G. C. A1 - Winchester, M. A1 - Miura, T. A1 - Methven, B. A1 - Sturgeon, R. A1 - Jährling, R. A1 - Rienitz, O. A1 - Mariassy, M. A1 - Hankova, Z. A1 - Sobina, E. A1 - Krylov, A. I. A1 - Kustikov, Y. A. A1 - Smirnov, V. V. T1 - Establishing comparability and compatibility in the purity assessment of high purity zinc as demonstrated by the CCQM-P149 intercomparison N2 - For the first time, an international comparison was conducted on the determination of the purity of a high purity element. Participants were free to choose any analytical approach appropriate for their institute’s applications and services. The material tested was a high purity zinc, which had earlier been assessed for homogeneity and previously used in CCQM-K72 for the determination of six defined metallic impurities. Either a direct metal assay of the Zn mass fraction was undertaken by EDTA titrimetry, or an indirect approach was used wherein all impurities, or at least the major ones, were determined and their sum subtracted from ideal purity of 100 %, or 1 kg/kg. Impurity assessment techniques included glow discharge mass spectrometry, inductively coupled plasma mass spectrometry and carrier gas hot extraction/combustion analysis. Up to 91 elemental impurities covering metals, non-metals and semi-metals/metalloids were quantified. Due to the lack of internal experience or experimental capabilities, some participants contracted external laboratories for specific analytical tasks, mainly for the analysis of non-metals. The reported purity, expressed as zinc mass fraction in the high purity zinc material, showed excellent agreement for all participants, with a relative standard deviation of 0.011 %. The calculated reference value, w(Zn) = 0.999 873 kg/kg, was assigned an asymmetric combined uncertainty of + 0.000025 kg/kg and – 0.000028 kg/kg. Comparability amongst participating metrology institutes is thus demonstrated for the purity determination of high purity metals which have no particular difficulties with their decomposition / dissolution process when solution-based analytical methods are used, or which do not have specific difficulties when direct analysis approaches are used. Nevertheless, further development is required in terms of uncertainty assessment, quantification of non-metals and the determination of purity of less pure elements and/or for those elements suffering difficulties with the decomposition process. KW - Purity assessment KW - Direct metal assay KW - Impurity assessment KW - Non-metal analysis KW - High-purity elements KW - SI-traceability PY - 2018 DO - https://doi.org/10.1088/1681-7575/aaa677 SN - 1681-7575 SN - 0026-1394 VL - 55 IS - 2 SP - 211 EP - 221 PB - Institute of Physics Publishing CY - Bristol AN - OPUS4-44257 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rack, A. A1 - Riesemeier, Heinrich A1 - Zabler, S. A1 - Weitkamp, T. A1 - Müller, Bernd R. A1 - Weidemann, Gerd A1 - Modregger, P. A1 - Banhart, J. A1 - Helfen, L. A1 - Danilewsky, A.N. A1 - Gräber, H.G. A1 - Heldele, R. A1 - Mayzel, B. A1 - Goebbels, Jürgen A1 - Baumbach, T. ED - Stuart R. Stock, T1 - The high-resolution synchrotron-based imaging stations at the BAMline (BESSY) and TopoTomo (ANKA) N2 - The BAMline at the BESSY light source in Berlin and the TopoTomo beamline at the ANKA synchrotron facility in Karlsruhe (both Germany) operate in the hard X-ray regime (above 6 keV) with similiar photon flux density. For typical imaging applications, a double multilayer monochromator or a filtered white beam is used. In order to optimise the field of view and the resolution of the available indirect pixel detectors, different optical systems have been installed, adapted, respectively, to a large field of view (macroscope) and to high spatial resolution (microscope). They can be combined with different camera systems, ranging from 16-bit dynamic range slow-scan CCDs to fast CMOS cameras. The spatial resolution can be brought substantially beyond the micrometer limit by using a Bragg magnifier. The moderate flux of both beamlines compared to other 3rd generation light sources is compensated by a dedicated scintillator concept. For selected applications, X-ray beam collimation has proven to be a reliable approach to increase the available photon flux density. Absorption contrast, phase contrast, holotomography and refraction-enhanced imaging are used depending on the application. Additionally, at the TopoTomo beamline digital white beam synchrotron topography is performed, using the digital X-ray pixel detectors installed. KW - Microtomography KW - Non-destructive evaluation KW - Coherent imaging KW - X-ray refraction KW - X-ray phase contrast KW - Synchrotron-CT KW - Synchrotron instrumentation KW - Scintillator KW - Bragg magnification KW - Holotomography KW - X-ray topography PY - 2008 DO - https://doi.org/10.1117/12.793721 SN - 0277-786X VL - 7078 SP - 70780X-1 - 70780X-9 AN - OPUS4-18296 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lange, T. A1 - Heinrich, Sebastian A1 - Liebner, Christian A1 - Hieronymus, Hartmut A1 - Klemm, E. T1 - Reaction engineering investigations of the partial oxidation of o-xylene in the explosion regime - microfixed bed versus catalyst coating N2 - The selective gas phase oxidation of o-xylene was investigated inside of the explosion regime using a microstructured reactor. The V2O5/TiO2 catalyst was used as microfixed bed and as catalyst coating. There were no significant losses of the selectivity to phthalic anhydride with feed compositions up to 7 vol % o-xylene observable. Above 7 vol % the selectivity decreased due to total oxidation, especially for the microfixed bed, which was probably caused by a hotspot. KW - Catalysis KW - Microreactors KW - Partial oxidation KW - Xylene KW - o-Xylene KW - Explosion regime PY - 2013 DO - https://doi.org/10.1002/cite.201200197 SN - 0009-286X SN - 1522-2640 VL - 85 IS - 4 SP - 461 EP - 466 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-30298 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fretwurst, T. A1 - Buzanich, Günter A1 - Nahles, S. A1 - Woelber, J. P. A1 - Riesemeier, Heinrich A1 - Nelson, K. T1 - Metal elements in tissue with dental peri-implantitis: a pilot study N2 - Objectives: Dental peri-implantitis is characterized by a multifactorial etiology. The role of metal elements as an etiological factor for peri-implantitis is still unclear. The aim of this study was to investigate the incidence of metal elements in bone and mucosal tissues around dental Grade 4 CP titanium implants with signs of peri-implantitis in human patients. Methods: In this prospective pilot study, all patients were enrolled consecutively in two study centers. Bone and soft tissue samples of patients with peri-implantitis with indication for explantation were analyzed for the incidence of different elements (Ca, P, Ti, Fe) by means of synchrotron radiation X-ray fluorescence spectroscopy (SRXRF) and polarized light microscopy (PLM). The existence of macrophages and lymphocytes in the histologic specimens was analyzed. Results: Biopsies of 12 patients (seven bone samples, five mucosal samples) were included and analyzed. In nine of the 12 samples (75%), the SRXRF examination revealed the existence of titanium (Ti) and an associated occurrence with Iron (Fe). Metal particles were detected in peri- implant soft tissue using PLM. In samples with increased titanium concentration, lymphocytes were detected, whereas M1 macrophages were predominantly seen in samples with metal particles. Conclusion: Titanium and Iron elements were found in soft and hard tissue biopsies retrieved from peri-implantitis sites. Further histologic and immunohistochemical studies need to clarify which specific immune reaction metal elements/particles induce in dental peri-implant tissue. KW - Peri-implantitis KW - Metal elements KW - Synchrotron radiation X-ray fluorescence PY - 2016 DO - https://doi.org/10.1111/clr.12718 SN - 0905-7161 VL - 27 IS - 9 SP - 1178 EP - 1186 PB - WILEY-BLACKWELL CY - 111 RIVER ST, HOBOKEN 07030-5774, NJ USA AN - OPUS4-38641 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lange, T. A1 - Neher, F. A1 - Klemm, E. A1 - Heinrich, Sebastian A1 - Balcazar Pust, Emilio A1 - Liebner, Christian A1 - Hieronymus, Hartmut T1 - Heterogeneous catalysis meets micro reactors: Partial oxidations in the explosion regime N2 - Investigations on primary, secondary and tertiary explosion protection have been performed for micro reactors with slit-like channels which are coated with catalyst. Ethene/oxygen mixtures have been used as model gas mixtures representing explosion group IIB (DIN EN ISO 16852). It could be shown that the explosion regime can be significantly reduced when using micro reactors (primary explosion protection). Furthermore, safe Operation inside the explosion regime is possible with micro reactors (secondary explosion protection), but, at certain conditions thermal runaway and ignition of detonations are possible. An unexpected behaviour has been found, because thermal runaway occurred when Volumetrie flow rate was increased. This behaviour is completely opposite to that of multi tube fixed bed reactors which show an increase of safety when increasing volumetric flow rate. Micro reactors can be constructed pressure-resistant even when detonations occur inside (tertiary explosion protection). For the example of o-xylene oxidation it could be shown that space time yield can be increased significantly when entering explosion regime. T2 - DGMK International conference - Selective oxidation and functionalization: Classical and alternative routes and sources CY - Berlin, Germany DA - 13.10.2014 PY - 2014 SN - 978-3-941721-44-9 VL - 2014-3 SP - 97 EP - 105 AN - OPUS4-31759 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Holzweber, Markus A1 - Heinrich, T. A1 - Kunz, V. A1 - Richter, S. A1 - Traulsen, C.H.-H. A1 - Schalley, C.A. A1 - Unger, Wolfgang T1 - Principal component analysis (PCA)-assisted time-of-flight secondary-ion mass spectrometry (ToF-SIMS): a versatile method for the investigation of self-assembled monolayers and multilayers as precursors for the bottom-up approach of nanoscaled devices N2 - The production of high-quality self-assembled monolayers (SAMs) followed by layer-by-layer (LbL) self-assembly of macrocycles is essential for nanotechnology applications based on functional surface films. To help interpret the large amount of data generated by a standard ToF-SIMS measurement, principal component analysis (PCA) was used. For two examples, the advantages of a combination of ToF-SIMS and PCA for quality control and for the optimization of layer-by-layer self-assembly are shown. The first example investigates how different cleaning methods influence the quality of SAM template formation. The second example focuses on the LbL self-assembly of macrocycles and the corresponding stepwise surface modification. KW - ToF-SIMS KW - Principal component analysis KW - Self assembled monolayer KW - Layer by layer PY - 2014 DO - https://doi.org/10.1021/ac500059a SN - 0003-2700 SN - 1520-6882 VL - 86 IS - 12 SP - 5740 EP - 5748 PB - American Chemical Society CY - Washington, DC AN - OPUS4-30963 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Liebner, Christian A1 - Hieronymus, Hartmut A1 - Heinrich, Sebastian A1 - Edeling, Florian A1 - Lange, T. A1 - Klemm, E. ED - Beyer, M. ED - Stolz, T. T1 - Zündung, Ausbreitung und Unterdrückung von Explosionen in einem Mikroreaktor N2 - Der vorliegende Beitrag behandelt spezifische Aspekte der Sicherheitstechnik bei heterogen katalysierten Oxidationsreaktionen. Ergebnisse von Explosionsuntersuchungen an Ethen-Sauerstoffgemischen in einem kontinuierlich betriebenen Mikroreaktor, die beispielsweise für den Ethylenoxidprozess relevant sind, werden vorgestellt. Der Anfangsdruck der untersuchten Eduktgemische lag zwischen 1000 hPa und 10000 hPa bei Anfangstemperaturen zwischen Umgebungstemperatur und einer Temperatur bis zu 673 K. Mikrostrukturierte Reaktoren bieten einen erweiterten Bereich von Betriebsbedingungen. Die Untersuchungen zielen auf den sicheren Betrieb eines Mikroreaktors bei Bedingungen, die bei konventionellen Reaktoren als innerhalb des Explosionsbereichs eingestuft werden, ab. In bestimmten Grenzen kann eine Unterdrückung von Explosionen in einem Mikroreaktor erreicht werden. Es ist jedoch nicht möglich, einen Mikroreaktor unter allen Bedingungen sicher zu betreiben. Aus diesen Gründen wurde die Explosionsausbreitung durch einen mikrostrukturierten Reaktor hindurch und die Zündung einer Gasphasenexplosion durch Hot-Spots in dem Reaktor untersucht. Die angewandten Untersuchungsmethoden sind Gegenstand aktueller Normungsaktivitäten. T2 - 13. BAM-PTB-Kolloquium zur chemischen und physikalischen Sicherheitstechnik CY - Braunschweig, Germany DA - 18.06.2013 KW - Micro Reactor KW - Explosion KW - Safety PY - 2013 SN - 978-3-95606-062-5 DO - https://doi.org/10.7795/210.20130910K SN - 1868-5838 SP - 90 EP - 98 AN - OPUS4-29849 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rack, T. A1 - Zabler, S. A1 - Rack, A. A1 - Riesemeier, Heinrich A1 - Nelson, K. T1 - An in vitro pilot study of the abutment stability during loading in virgin and fatigue-loaded conical dental implants using synchrotron-based radiography N2 - Purpose: The implant-abutment connection of a two-piece dental implant exhibits complex micromechanical behavior. A microgap is evident at the implant-abutment interface, even in the virgin state, and its width varies when an external mechanical load is applied. Materials and Methods: This study used high-resolution synchrotron-based radiography in combination with hard x-ray phase-contrast mode to visualize this gap and estimate its size. Commercially available implants with different internal conical implant-abutment connections were imaged. Pairs of implants were imaged as manufactured (new) and after fatigue loading (5 million cycles up to 120 N). Then, different static loads were applied at different angles relative to the implant-abutment assemblies, and the implant-abutment microgaps were measured and compared. Results: Microgaps existed in all systems. Fatigue loading extended the size of the microgap and increased the possibility of micromovement of the implant-abutment complex. The cone angle of the connection also influenced the stability of the abutment, with flatter cones appearing to be more stable. Conclusion: Cyclic loading at medium force (120 N) induces plastic deformation of titanium implants and abutments. KW - Dental implants KW - Digital radiography KW - Phase-contrast microscopy KW - Synchrotron radiography KW - Titanium PY - 2013 DO - https://doi.org/10.11607/jomi.2748 SN - 0882-2786 SN - 1942-4434 VL - 28 IS - 1 SP - 44 EP - 50 PB - Quintessence Publ. Co. CY - Lombard, Ill. AN - OPUS4-30546 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rack, A. A1 - Stiller, M. A1 - Nelson, K. A1 - Knabe, C. A1 - Rack, T. A1 - Zabler, S. A1 - Dalügge, O. A1 - Riesemeier, Heinrich A1 - Cecilia, A. A1 - Goebbels, Jürgen T1 - Ex vivo and in vitro synchrotron-based micro-imaging of biocompatible materials applied in dental surgery N2 - Biocompatible materials such as porous bioactive calcium phosphate ceramics or titanium are regularly applied in dental surgery: ceramics are used to support the local bone regeneration in a given defect, afterwards titanium implants replace lost teeth. The current gold standard for bone reconstruction in implant dentistry is the use of autogenous bone grafts. But the concept of guided bone regeneration (GBR) has become a predictable and well documented surgical approach using biomaterials (bioactive calcium phosphate ceramics) which qualify as bone substitutes for this kind of application as well. We applied high resolution synchrotron microtomography and subsequent 3d image analysis in order to investigate bone formation and degradation of the bone substitute material in a three-dimensional manner, extending the knowledge beyond the limits of classical histology. Following the bone regeneration, titanium-based implants to replace lost teeth call for high mechanical precision, especially when two-piece concepts are used in order to guaranty leak tightness. Here, synchrotron-based radiography in comparison with classical laboratory radiography yields high spatial resolution in combination with high contrast even when exploiting micro-sized features in these kind of highly attenuating objects. Therefore, we could study micro-gap formation at interfaces in two-piece dental implants with the specimen under different mechanical load. We could prove the existence of micro-gaps for implants with conical connections as well as to study the micromechanical behavior of the mating zone of conical implants during loading. The micro-gap is a potential issue of failure, i. e. bacterial leakage which can induce an inflammatory process. T2 - SPIE Conference 7804 - Developments in X-ray tomography VII CY - San Diego, CA, USA DA - 2010-08-02 KW - Microtomography KW - Synchrotron radiation KW - Radiography KW - Dental implants KW - Bioceramics KW - Implant-abutment interface PY - 2010 DO - https://doi.org/10.1117/12.858435 SN - 0277-786X N1 - Serientitel: SPIE proceedings series – Series title: SPIE proceedings series VL - 7804 SP - 78040E-1 - 78040E-8 AN - OPUS4-22731 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rack, A. A1 - Rack, T. A1 - Stiller, M. A1 - Riesemeier, Heinrich A1 - Zabler, S. A1 - Nelson, K. T1 - In vitro synchrotron-based radiography of micro-gap formation at the implant-abutment interface of two-piece dental implants N2 - Micro-gap formation at the implant-abutment interface of two-piece dental implants was investigated in vitro using high-resolution radiography in combination with hard X-ray synchrotron radiation. Images were taken with the specimen under different mechanical loads of up to 100 N. The aim of this investigation was to prove the existence of micro-gaps for implants with conical connections as well as to study the mechanical behavior of the mating zone of conical implants during loading. Synchrotron-based radiography in comparison with classical laboratory radiography yields high spatial resolution in combination with high contrast even when exploiting micro-sized features in highly attenuating objects. The first illustration of a micro-gap which was previously indistinguishable by laboratory methods underlines that the complex micro-mechanical behavior of implants requires further in vitro investigations where synchrotron-based micro-imaging is one of the prerequisites. KW - X-ray imaging KW - Dental implants KW - Digital radiography KW - Implant-abutment interface PY - 2010 DO - https://doi.org/10.1107/S0909049510001834 SN - 0909-0495 SN - 1600-5775 VL - 17 IS - 2 SP - 289 EP - 294 PB - Blackwell Publishing CY - Oxford AN - OPUS4-22121 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Jörg A1 - Martin, Sven A1 - Mädebach, Heinrich A1 - Urech, L. A1 - Lippert, T. A1 - Wokaun, A. A1 - Kautek, Wolfgang T1 - Femto- and nanosecond laser treatment of doped polymethylmethacrylate N2 - Femto- and nanosecond laser ablation of polymethylmethacrylate (PMMA) and PMMA doped with a linear absorber was investigated in the infrared spectral region. Ablation thresholds were determined and incubation phenomena were identified. The ‘degree’ of incubation was calculated employing a phenomenological model. The influence of the pulse duration on the machining quality of the polymers was examined. The presence of an absorbing chromophore is not a prerequisite for a controllable fs-laser structuring in contrast to the ns-treatment. Surface swelling always accompanied ablation. KW - Laser ablation KW - Laser beam machining KW - Doping thin films KW - Polymers-radiation effects PY - 2005 DO - https://doi.org/10.1016/j.apsusc.2005.01.078 SN - 0169-4332 SN - 1873-5584 VL - 247 SP - 406 EP - 411 PB - North-Holland CY - Amsterdam AN - OPUS4-7470 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Urech, L. A1 - Lippert, T. A1 - Wokaun, A. A1 - Martin, Sven A1 - Mädebach, Heinrich A1 - Krüger, Jörg T1 - Removal of doped poly(methylmetacrylate) from tungsten and titanium substrates by femto- and nanosecond laser cleaning N2 - The influence of different laser pulse lengths on the removal of a polymer layer from metal substrates was investigated. As model systems, doped poly(methylmetacrylate) (PMMA) on titanium and tungsten substrates were selected. The ablation threshold and irradiation spot morphology of titanium and tungsten were compared for femtosecond (fs) and nanosecond (ns) laser irradiation and different pulse numbers. Nanosecond laser treatment resulted in a non-homogeneous surface morphology for both titanium and tungsten substrates. Femtosecond irradiation of tungsten revealed a homogeneous ablation spot with little changes in the surface morphology. For titanium, the formation of columnar structures within the irradiation spot was observed. Two different dopant concentrations were used for PMMA to achieve an equal linear absorption coefficient for the femto- and nanosecond laser wavelengths of 790 and 1064 nm. The best results were achieved for the removal of doped PMMA by femtosecond laser irradiation, where only a minimal modification of the metal surface was detected. In the case of nanosecond laser exposure, a pronounced change of the structure was observed, suggesting that damage-free cleaning of the selected metal may only be possible using femtosecond laser pulses. Different experimental parameters, such as laser fluence, pulse repetition rate and sample speed were also investigated to optimize the cleaning quality of doped PMMA from tungsten substrates with femtosecond laser pulses. KW - Poly(methylmetacrylate) KW - Laser treatment KW - Tungsten KW - Titanium KW - Femtosecond PY - 2006 DO - https://doi.org/10.1016/j.apsusc.2005.07.109 SN - 0169-4332 SN - 1873-5584 VL - 252 IS - 13 SP - 4754 EP - 4758 PB - North-Holland CY - Amsterdam AN - OPUS4-12368 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hieronymus, Hartmut A1 - Fischer, J. A1 - Heinrich, Sebastian A1 - Liebner, Christian A1 - Lange, T. A1 - Klemm, E. T1 - Sicherheitstechnische Untersuchungen zum Betrieb von Mikroreaktoren im Explosionsbereich N2 - Es wird eine Methode zur sicherheitstechnischen Untersuchung von Mikroreaktoren und mikrostrukturierten Komponenten, die im Explosionsbereich betrieben werden sollen, vorgestellt. Mikrostrukturierte Reaktoren sind nicht inhärent sicher, wenngleich der Bereich der sicheren Betriebsbedingungen gegenüber konventionellen Reaktoren erweitert ist. Der Explosionsbereich kann durch die Mikrostrukturen eingeengt werden. Am Beispiel von Ethylen/Sauerstoff-Gemischen und Ethylen/N2O-Gemischen wird hinsichtlich der Ausbreitung von Detonationen durch Kapillarrohre gezeigt, dass die sogenannte λ/3-Regel angewandt werden kann. Darüber hinaus werden erste Ergebnisse der Untersuchung der Ausbreitung von Explosionen durch einen Mikroreaktor mit rechteckigem Strömungskanal vorgestellt. KW - Detonationszellbreite KW - Explosionsgrenzen KW - Mikroreaktoren KW - Sicherheitstechnik KW - Detonation cell width KW - Explosion limit KW - Microreactor KW - Saftey engineering PY - 2011 DO - https://doi.org/10.1002/cite.201100112 SN - 0009-286X SN - 1522-2640 VL - 83 IS - 10 SP - 1742 EP - 1747 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-24486 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rack, T. A1 - Zabler, S. A1 - Rack, C. A1 - Stiller, M. A1 - Riesemeier, Heinrich A1 - Cecilia, A. A1 - Nelson, K. T1 - Coherent synchrotron-based micro-imaging employed for studies of micro-gap formation in dental implants N2 - Biocompatible materials such as titanium are regularly applied in oral surgery. Titanium-based implants for the replacement of missing teeth demand a high mechanical precision in order to minimize micro-bacterial leakage, especially when two-piece concepts are used. Synchrotron-based hard x-ray radiography, unlike conventional laboratory radiography, allows high spatial resolution in combination with high contrast even when micro-sized features in such highly attenuating objects are visualized. Therefore, micro-gap formation at interfaces in two-piece dental implants with the sample under different mechanical loads can be studied. We show the existence of micro-gaps in implants with conical connections and study the mechanical behavior of the mating zone of conical implants during loading. The micro-gap is a potential source of implant failure, i.e., bacterial leakage, which can be a stimulus for an inflammatory process. T2 - 10th International conference on X-ray microscopy CY - Chicago, Illinois, USA DA - 15.08.2010 KW - X-ray imaging KW - Dental implants KW - Digital radiography KW - Implant-abutment interface KW - Synchrotron radiation KW - X-ray phase contrast PY - 2011 SN - 978-0-7354-0925-5 DO - https://doi.org/10.1063/1.3625398 N1 - Serientitel: AIP conference proceedings – Series title: AIP conference proceedings VL - 1365 SP - 445 EP - 448 AN - OPUS4-25347 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Liebner, Christian A1 - Heinrich, Sebastian A1 - Edeling, Florian A1 - Hieronymus, Hartmut A1 - Lange, T. A1 - Klemm, E. ED - Pierucci, S. ED - Klemes, J.J. ED - De Rademaeker, E. ED - Fabiano, B. ED - Buratti, S.S. T1 - Explosion initiation, propagation, and suppression inside a micro structured reactor N2 - The present contribution reports on specific aspects of safety engineering in heterogeneously catalysed oxidation reactions. Results for ethene-oxygen-mixtures in a continuous-flow micro reactor are reported related to the safety issues of the ethylene oxide process. Initial pressure is ranging from below 1 bar up to 10 bar at initial temperatures ranging from room temperature up to 673 K. Micro structured reactors offer an extended range of operating conditions. The key issue to be discussed in the present contribution is how to safely operate a micro reactor at conditions in conventional devices to be characterised as inside the explosion region. Within certain limits suppression of explosion inside a micro reactor can be achieved. This holds true for chain reactions as well as runaway reactions. Nevertheless it is not possible to safely operate micro structured reactors at any condition. Therefore, explosion propagation through a Micro structured reactor and initiation of gas phase explosions by hot spots inside the reactor were investigated. The investigation methods applied are subject to actual standardization. T2 - 14th International symposium on loss prevention and safety promotion in the process industries CY - Florence, Italy DA - 12.05.2013 KW - Micro reactor KW - Explosion KW - Safety PY - 2013 SN - 978-88-95608-22-8 DO - https://doi.org/10.3303/CET1331101 SN - 1974-9791 N1 - Serientitel: Chemical engineering transactions – Series title: Chemical engineering transactions IS - 31 SP - 601 EP - 606 PB - AIDIC, Associazione Italiana di Ingegneria Chimica CY - Milano AN - OPUS4-28583 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lange, T. A1 - Heinrich, Sebastian A1 - Liebner, Christian A1 - Hieronymus, Hartmut A1 - Klemm, E. T1 - Partial oxidation of o-xylene to phthalic anhydride inside of the explosion regime using a micro structured reactor N2 - The heterogeneously catalyzed gas phase oxidation of o-xylene (oX) to phthalic anhydride (PA) was investigated above the lower explosion limit of appr. 2 vol.% oxylene in air using a micro structured reactor. For these investigations a V2O5/T1O2 grafting catalyst was applied as micro fixed bed and as wall catalyst. Up to 7 voL% 0-xylene, selectivities as well as space-time-yields to PA could be increased siginificantly. At o-xylene concentrations higher than 7 vol. %, the selectivity and space-time-yield to PSA decreased, probably due to a hotspot, which was predicted at high o-xylene concentrations with an approximation and could be indirectly approved by thermal deactivation of the used catalyst. T2 - 2012 AIChE Annual meeting CY - Pittsburgh, PA, USA DA - 28.10.2012 KW - O-xylene oxidation KW - V2O5/TiO2 catalyst KW - Micro structured reactor KW - Explosion regime KW - Micro reactor KW - Explosion KW - Phthalic anhydride KW - Partial oxidation PY - 2013 SN - 9781622767380 SP - 90 EP - 93 AN - OPUS4-28706 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - 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 -