TY - CONF A1 - Meyer-Plath, Asmus T1 - Plasmaunterstützte Modifizierung von Kohlenstoffanoröhren T2 - 1. Workshop der Innovationsallianz Carbon Nanotubes CY - Leverkusen, Germany DA - 2009-01-26 PY - 2009 AN - OPUS4-18723 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Schulze, Rolf-Dieter A1 - Meyer-Plath, Asmus A1 - Joshi, Ranjit A1 - Wettmarshausen, Sascha T1 - New Plasma Techniques for Polymer Surface Modification with Monotype Functional Groups N2 - The production of chemically-defined plasma polymers and the introduction of monotype functional groups onto polymer surfaces are described. One method is to lower the energetic level of low-pressure plasmas. Pressure- and plasma-pulsed plasmas were successfully tested for the production of chemically-defined plasma polymers by increasing the monomer supply during the plasma-off period. Well-defined ultra-thin polymer films with regular structure were deposited from atmospheric plasmas by electrospray techniques. Post-plasma wet-chemical processing was also applied, as were gas/liquid-based aerosols and underwater plasmas. KW - Plasma KW - Polymer-Oberflächenfunktionalisierung KW - Macromolecular plasma KW - Monotype functional groups KW - Plasma bromination KW - Plasma treatment KW - Pressure-pulsed plasma KW - Underwater plasma PY - 2008 DO - https://doi.org/10.1002/ppap.200700145 SN - 1612-8850 SN - 1612-8869 VL - 5 IS - 5 SP - 407 EP - 423 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-17742 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Plasma-Thermal Expansion and Chemical Functionalization of Graphite Intercalation Compounds T2 - 2009 International Conference on Carbon "CARBON 2009" CY - Biarritz, France DA - 2009-06-15 PY - 2009 AN - OPUS4-19620 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Plasma-Thermal Modification of Graphites T2 - 1st German-Japanese Joint Symposium on Development and Technology of Carbon Materials CY - Meitingen, Germany DA - 2009-06-22 PY - 2009 AN - OPUS4-19621 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Physikalisch-Chemische Charakterisierung von CNT T2 - Workshop "Charakterisierung von CNT-Materialien" CY - Berlin, Germany DA - 2009-07-01 PY - 2009 AN - OPUS4-19625 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Highly effective purification of carbon nanotubes by plasma-thermal annealing T2 - NT 10 - 11th International Conference on the Science and Application of Nanotubes CY - Montreal, Canada DA - 2010-06-27 PY - 2010 AN - OPUS4-21568 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Removal of metal impurities by plasma-thermal gas-phase purification of carbon nanotubes T2 - Carbon 2010 - The Annual World Conference on Carbon CY - Clemson, SC, USA DA - 2010-07-11 PY - 2010 AN - OPUS4-21714 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Highly effective purification of carbon nanotubes by plasma-thermal annealing T2 - Inno. CNT Jahrestagung CY - Ettlingen, Germany DA - 2011-01-25 PY - 2011 AN - OPUS4-23093 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Wettmarshausen, Sascha A1 - Mix, Renate A1 - Meyer-Plath, Asmus A1 - Mittmann, Hans-Ulrich A1 - Friedrich, Jörg Florian ED - K.L. Mittal, T1 - Plasma Bromination - a selective way to monotype functionalized polymer surfaces KW - Functional groups KW - Polymer surfaces KW - Plasma bromination KW - Grafting KW - Spacer KW - Selective plasma process PY - 2009 SN - 978-90-04-16590-8 VL - 5 SP - 3 EP - 18 PB - Koninklijke Brill NV CY - Leiden, The Netherlands AN - OPUS4-18944 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Joshi, Ranjit A1 - Schulze, Rolf-Dieter A1 - Meyer-Plath, Asmus A1 - Friedrich, Jörg Florian T1 - Selective surface modification of Poly(propylene) with OH and COOH groups using liquid-plasma systems N2 - Underwater plasma and glow discharge electrolysis are interesting new methods for polymer surface functionalization. The achievable content of O-containing functional groups exceeds that of oxygen glow discharge gas plasmas by a factor of two (up to ca. 56 O/100 C). The percentage of OH groups among all O-containing groups can reach 25 to 40%, whereas it is about 10% in the gas plasmas. Addition of hydrogen peroxide increases the fraction of OH groups to at most 70% (27 OH/100 C). The liquid plasma systems are also able to polymerize acrylic acid and deposit the polymer as very thin film on substrate surfaces or membranes, thereby retaining about 80% of all COOH functional groups (27 COOH/100 C). KW - Polymeroberflächen KW - Funktionelle Gruppen PY - 2008 DO - https://doi.org/10.1002/ppap.200700175 SN - 1612-8850 SN - 1612-8869 VL - 5 IS - 7 SP - 695 EP - 707 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-18884 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Selektive Aminofunktionalisierung von Polymeroberflächen: Niederdruck-Plasmaprozesse im Vergleich zu UV-Laser-Funktionalisierung T2 - Vakuumbeschichtung und Plasmaoberflächentechnik CY - Dresden, Germany DA - 2009-10-20 PY - 2009 AN - OPUS4-20347 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Joshi, Ranjit A1 - Schulze, Rolf-Dieter A1 - Meyer-Plath, Asmus A1 - Wagner, M.H. A1 - Friedrich, Jörg Florian T1 - Selective surface modification of polypropylene using underwater plasma technique or underwater capillary discharge N2 - Among new types of plasma processes, the underwater plasma is one of the most attractive methods for functionalization of polymer surfaces. The interesting features of plasma solution system are that the material surfaces to be modified remain in contact with the plasma-moderated solution. The role of plasma-moderated liquids, allows the reach of the reactive species through solution onto the geometrically hindered sites. The UV radiation produced in plasma formation helps in generating additional excited, ionized, and dissociated molecules and species in the reaction solution. An interesting feature of the technique is its flexibility to use a wide variety of additives as or in solution system. This allows us to create a selective or monotype functionalization of material surfaces. Such system was studied for the selective hydroxyl functionalization of polypropylene surface. The oxidation of polymer surfaces and the introduction of O-containing functional groups by underwater plasma was found to exceed concentrations typically achieved in oxygen low-pressure gas discharge plasmas up-to two-folds (maximal 56 O/100 C). The fraction of OH groups among all O-containing moieties amounts from 25 to 40% in comparison to that in the gas plasma of about 10% OH groups. Addition of hydrogen peroxide into this same system increases the fraction of C—O bonds up to 75% (27-OH/100 O). A study was focused to optimize the role of hydrogen peroxide on the efficiency of oxidation and selectivity with chemical derivatization with respect to the formation of mono-sort hydroxyl functionalities, calculated using a chemical derivatization technique. KW - Capillary discharge KW - Functionalization of polymer KW - Modification surfaces KW - Underwater plasma KW - Surface modification KW - Polymer functionalization PY - 2009 DO - https://doi.org/10.1002/ppap.200930601 SN - 1612-8850 SN - 1612-8869 VL - 6 IS - Suppl. 1 SP - 5218 EP - 5222 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-22772 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - CarbonNanotubes: Synthesis, Functionalization, Dispersion T2 - International Nanotechnology Exhibition and Conference Nano Tech 2011 CY - Tokyo, Japan DA - 2011-02-16 PY - 2011 AN - OPUS4-23233 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hanelt, Sven A1 - Orts Gil, Guillermo A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus T1 - Differentiation and quantification of surface acidities on MWCNTs by indirect potentiometric titration N2 - Wet-chemically oxidized carbon nanotubes (CNTs) generally exhibit both covalently-bound acidic functional groups on the surface and surface-adsorbed acidic substances, i.e. carbonaceous CNT fragments from the oxidation procedure. Direct potentiometric titration of oxidizable high surface area materials with dynamically desorbing acidic fragments is slow and inaccurate. Adsorbed acidic fragments are deprotonated by sodium hydroxide and form anions in solution which is not the case for covalently bound acidic groups on the CNTs, so the following filtration after NaOH treatment separates desorbable acidic substances from non-desorbable or covalently bound groups. For a known concentration of NaOH, titration of the eluate with hydrochloric acid (HCl) allows determination of the concentrations of both types of acidities. However, contrary to reports in the literature, the NaOH consumed by non-desorbed acidic groups has to be accounted for and impedes distinction of desorbed acidic groups via their pKa values. Results are presented of a study on the information content and the reliability of indirect potentiometric Boehm titration for different oxidized multi-walled CNTs. PY - 2011 DO - https://doi.org/10.1016/j.carbon.2011.03.016 SN - 0008-6223 SN - 1873-3891 VL - 49 IS - 9 SP - 2978 EP - 2988 PB - Pergamon Press CY - New York, NY AN - OPUS4-23625 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Plasmachemische Modifizierung von Graphiten T2 - Herbsttagung 2008 des Arbeitskreis Kohlenstoff in der Deutschen Keramischen Gesellschaft e. V. CY - Hanau, Germany DA - 2008-10-30 PY - 2008 AN - OPUS4-18182 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Ebert, H.-P. A1 - Reichenauer, G. A1 - Brandt, R. A1 - Braxmeier, S. A1 - Bauer, T. A1 - Tamme, R. A1 - Langer, W. A1 - Hudler, B. A1 - Christ, M. A1 - Sextl, G. A1 - Müller, G. A1 - Helbig, U. A1 - Houbertz, R. A1 - Voigt, W. A1 - Schmidt, H. A1 - Zehl, T. A1 - Mach, Reinhard A1 - Maneck, Heinz-Eberhard A1 - Meyer-Plath, Asmus A1 - Oleszak, Franz A1 - Keuper, M. A1 - Reisert, M. A1 - Burkhardt, H. A1 - Günther, E. A1 - Mehling, H. T1 - Netzwerk zur Überwindung grundlegender Probleme bei der Entwicklung hocheffizienter Latentwärmespeicher auf Basis anorganischer Speichermaterialien KW - Latentwärmespeicher KW - Materialforschung KW - Plasmaverfahren KW - Graphit PY - 2008 SN - 978-3-00-024699-9 SP - 1 EP - 217 CY - Würzburg AN - OPUS4-18273 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus A1 - Mach, Reinhard A1 - Maneck, Heinz-Eberhard A1 - Oleszak, Franz A1 - Friedrich, Jörg Florian T1 - Plasma-chemical functionalization of expanded graphite T2 - International Conference on Carbon (Carbon 2008) CY - Nagano, Japan DA - 2008-06-13 KW - Gas Discharge Plasma KW - Expanded Graphite KW - Functionalization KW - Surface Chemistry PY - 2008 SP - 1 EP - 5 AN - OPUS4-18339 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus A1 - Mix, Renate A1 - Schulze, Rolf-Dieter A1 - Joshi, Ranjit ED - Tachibana, K. ED - Takai, O. T1 - New plasmas for polymer surface functionalization T2 - Proceedings of the 18th International Symposium on Plasma Chemistry (ISPC-18) CY - Kyoto, Japan DA - 2007-08-26 PY - 2007 SN - 978-4-9903773-4-2 SP - 29A/a8, 1 EP - 4 PB - International Union of Pure and Applied Chemistry CY - Kyoto AN - OPUS4-20666 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Mix, Renate A1 - Joshi, Ranjit A1 - Schulze, Rolf-Dieter A1 - Meyer-Plath, Asmus A1 - Friedrich, Jörg Florian ED - Tachibana, K. ED - Takai, O. T1 - Aerosol and underwater plasma for polymer surface functionalization T2 - Proceedings of the 18th International Symposium on Plasma Chemistry (ISPC-18) CY - Kyoto, Japan DA - 2007-08-26 PY - 2007 SN - 978-4-9903773-4-2 SP - 27P/80, 1 EP - 4 PB - International Union of Pure and Applied Chemistry CY - Kyoto AN - OPUS4-20667 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Physikalisch-chemische Charakterisierung von CNT T2 - Inno. CNT Jahrestagung CY - Marl (North Rhine-Westphalia), Germany DA - 2010-01-20 PY - 2010 AN - OPUS4-20860 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Wettmarshausen, Sascha A1 - Hanelt, Sven A1 - Mach, Reinhard A1 - Mix, Renate A1 - Zeynalov, Eldar A1 - Meyer-Plath, Asmus T1 - Plasma-chemical bromination of graphitic materials and its use for subsequent functionalization and grafting of organic molecules N2 - Plasma-chemical bromination has been shown to be well-suited for highly selective and efficient C–Br-functionalization of polyolefin surfaces and has now been applied to graphitic materials, including highly oriented pyrolytic graphite (HOPG), natural graphite, carbon nanotubes, and graphitized carbon fibres. In contrast to the radical substitution of hydrogen by bromine at hydrogen-terminated sp3-hybridized carbon, bromination of all-carbon bound sp2-hybridized carbon in graphene requires addition to aromatic double bonds. The related change of sp2 to sp3 hybridization of the carbon atoms involved helps to explain experimental results of a loss in surface planarity on brominated HOPG. Bromine concentrations of up to 50 bromine atoms per 100 C-atoms were achieved in elemental bromine vapour under low-pressure plasma conditions using low-energetic inductively coupled radio-frequency plasma excitation. The time scale of the bromination progress was found to increase with the specific surface area of the material. The results of plasma-chemical bromination are compared to that of wet-chemical electrophilic addition reactions, which achieved 28 Br per 100 C for MWCNT. The resulting C–Br bonds from plasma-chemical processing of graphitic materials were shown to be well-suited for hydroxyl functionalization and for grafting of organic molecules by nucleophilic substitution with 1,6-diaminohexane and (3-aminopropyl)triethoxysilane. PY - 2010 DO - https://doi.org/10.1016/j.carbon.2010.06.054 SN - 0008-6223 SN - 1873-3891 VL - 48 IS - 13 SP - 3884 EP - 3894 PB - Pergamon Press CY - New York, NY AN - OPUS4-21954 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Duan, X.R. A1 - Lange, H. A1 - Meyer-Plath, Asmus T1 - Absolute density distribution of H atoms in a large-scale microwave plasma reactor N2 - Absolute number densities and the spatial distribution of atomic hydrogen in a large-scale microwave plasma reactor were measured by means of two-photon absorption laser-induced fluorescence (LIF) with laser radiation at 205 nm. The microwave discharge was operated at 2.45 GHz with a maximum power of 2 kW. Absolute number densities were obtained by calibrating the LIF detection system via NO2 titration in a flow tube reactor and in the range from 0.5×1015 to 2.5×1015 cm-3. Compared to small-scale reactors with a volume-to-surface ratio less than 3 cm, this reactor has a relatively homogeneous spatial distribution of atomic hydrogen. The mole fraction of atomic hydrogen in hydrogen plasmas ranges from 10% to 20%. The gas temperature–volume effect plays an important role in the spatial distribution of atomic hydrogen in this reactor. PY - 2003 DO - https://doi.org/10.1088/0963-0252/12/4/307 SN - 0963-0252 SN - 1361-6595 VL - 12 SP - 554 EP - 560 PB - IOP Publ. CY - Bristol AN - OPUS4-2696 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus A1 - Retzko, Iris A1 - Kühn, Gerhard A1 - Mix, Renate ED - d'Agostino, R. T1 - Comparison of different plasmachemical processes for the formation of monotype functionalized polymer surfaces T2 - 16th International Symposium on Plasma Chemistry (ISPC-16) CY - Taormina, Italy DA - 2003-06-22 PY - 2003 IS - CD-ROM PB - Dep. of Chemistry, Univ. CY - Bari AN - OPUS4-2709 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Analysis of plasma-generated radicals on polymer surfaces T2 - 16th International Symposium on Plasma Chemistry CY - Taormina, Italy DA - 2003-06-22 PY - 2003 AN - OPUS4-3095 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Surface functionalization in ammonia microwave plasmas for biomedical applications T2 - 16th International Symposium on Plasma Chemistry CY - Taormina, Italy DA - 2003-06-22 PY - 2003 AN - OPUS4-3100 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - The Potential of Surface Radicals for Polymer Functionalization T2 - 16th International Symposium on Plasma Chemistry CY - Taormina, Italy DA - 2003-06-22 PY - 2003 AN - OPUS4-3084 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer-Plath, Asmus T1 - Radikalidentifizierung auf Polymeren nach Plasmabehandlung N2 - Radikale bilden den Ausgangspunkt für Reaktionen chemisch inerter Polymere. So kann der Einbau funktioneller chemischer Gruppen in eine Polymeroberfläche über Reaktionen mit funktionsgruppentragenden Partnern erfolgen, wenn die Oberfläche, die Reaktionspartner oder beide über Radikalcharakter verfügen. Dabei bestimmt die Reaktivität und Dichte der Radikale auf der Polymeroberfläche die Effizienz des Funktionalisierungsprozesses entscheidend mit. Nach dessen Abschluß erlangen nicht-abgesättigte Radikale, d. h. solche, die nicht an der Kopplungsreaktion teilgenommen haben, besondere Bedeutung. Sie können noch mit Luftsauerstoff zu Peroxiden reagieren und anschließend zu einer (unbeabsichtigten) Sekundärfunktionalisierung der Oberfläche mit allen denkbaren Arten sauerstoffhaltiger Gruppen führen. Aus diesen Gründen gewinnt der Nachweis von Radikalen auf Polymeroberflächen für derzeit in der Entwicklung befindliche Ansätze der hocheffizienten und/oder hoch einheitlichen Oberflächenfunktionalisierung zunehmend an Bedeutung. Es werden daher wichtige Verfahren zur Quantifizierung von Oberflächenradikalen vorgestellt. Ferner wird ein neuer Ansatz zur Ausrüstung von Polymeroberflächen mit Radikalen vorgestellt, die dann ihrerseits Ausgangspunkt von Funktionalisierungsreaktionen sein können. KW - Polymere KW - Radikale KW - Plasma KW - Oberflächenanalyse PY - 2004 DO - https://doi.org/10.1002/vipr.200400221 SN - 0947-076X SN - 1522-2454 VL - 16 IS - 3 SP - 118 EP - 125 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-5545 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Radikale auf plasmabehandelten Polymeroberflächen - Verfahren zur Erzeugung und Identifzierung T2 - 12. Neues Dresdner Vakuumtechnisches Kolloquium CY - Dresden, Germany DA - 2004-10-14 PY - 2004 AN - OPUS4-5538 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, P. A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus T1 - Gezielte chemische Funktionalisierung von porösen Materialien und Bauteilen aus der Mikrosystemtechnik T2 - Workshop Funktionalisierung von Oberflächen für die Biotechnologie CY - Dresden, Deutschland DA - 2003-03-11 PY - 2003 SP - 1(?) EP - 8(?) PB - EFDS CY - Dresden AN - OPUS4-6962 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, P. A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus T1 - Selective chemical modification of porous materials and films for bio-medical applications T2 - CIP 2003 ; 14th International Colloquium on Plasma Processes CY - Antibes, France DA - 2003-06-30 PY - 2003 SP - 1(?) EP - 4(?) PB - sfv, Sociéte Française du Vide CY - Paris AN - OPUS4-6963 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus A1 - Mix, Renate A1 - Kühn, Gerhard A1 - Friedrich, Jörg Florian ED - d'Agostino, R. T1 - The Potential of Surface Radicals for Polymer Functionalization T2 - 16th International Symposium on Plasma Chemistry (ISPC-16) CY - Taormina, Italy DA - 2003-06-22 PY - 2003 IS - CD-ROM PB - Dep. of Chemistry, Univ. CY - Bari AN - OPUS4-2612 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Finke, B. A1 - Meyer-Plath, Asmus A1 - Schröder, K. A1 - Ohl, A. ED - d'Agostino, R. T1 - Analysis of plasma-generated radicals on polymer surfaces N2 - Plasma functionalisation in gas phase like ammonia allows to equip polymer surfaces with amino functional groups. An important question of this functionalisation consists in the limited knowledge about heterogeneous interface reactions, especially radical formation and subsequent reaction processes. Useful analytical methods comparable to those avilable for gas phase reactions are scarce. Here we report on investigations on plasma generated C-radicals by NO-labelling, showing similatr effects for different plasmas. T2 - 16th International Symposium on Plasma Chemistry (ISPC-16) CY - Taormina, Italy DA - 2003-06-22 PY - 2003 IS - CD-ROM SP - 1 EP - 6(?) PB - Dep. of Chemistry, Univ. CY - Bari AN - OPUS4-2613 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schröder, K. A1 - Ihrke, R. A1 - Meyer-Plath, Asmus A1 - Finke, B. A1 - Diener, A. A1 - Nebe, B. A1 - Ohl, A. ED - d'Agostino, R. T1 - Surface functionalization in ammonia microwave plasmas for biomedical applications T2 - 16th International Symposium on Plasma Chemistry (ISPC-16) CY - Taormina, Italy DA - 2003-06-22 PY - 2003 IS - CD-ROM PB - Dep. of Chemistry, Univ. CY - Bari AN - OPUS4-2614 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - The potential of surface radicals for polymer functionalization T2 - ISPS-16 CY - Taormina, Italy DA - 2003-06-22 PY - 2003 AN - OPUS4-4199 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - The potential of surface radicals for polymmer functionalization T2 - ISPC-16 CY - Taormina, Italy DA - 2003-06-22 PY - 2003 AN - OPUS4-4201 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Amino Functionalization of Polymers by Plasma Processing for the Attachment of Biomolecules and Adhesion Promotion of Copper Films T2 - SECOND INTERNATIONAL SYMPOSIUM ON ADHESION ASPECTS OF THIN FILMS CY - Savannah, GA, USA DA - 2005-11-09 PY - 2005 AN - OPUS4-11466 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Amino functionalization of polymers by low-pressure plasma processing - status and perspectives T2 - Tenth International Conference on Plasma Surface Engineering CY - Garmisch-Partenkirchen, Germany DA - 2006-09-11 PY - 2006 AN - OPUS4-13040 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer-Plath, Asmus T1 - Identification of Surface Radicals on Polymers N2 - Radicals can initiate reactions of chemically inert polymers. The incorporation of functional chemical groups to polymer surface can proceed via trapping or quenching reactions of polymer radicals with functionalized reaction partners. The density and reactivity of surfaces radicals governs the efficiency of the surface functionalization process. Subsequent to its termination, surviving, i.e. unreacted, radicals gain special importance since they exhibit a strong tendency to react with oxygen from the air. This generally will result in an unintended secondary functionalization of the polymer surface consisting of various oxygen groups. Therefore, the identification and quantification of radicals on polymer surfaces is becoming increasingly important for the on-going development of highly efficient and highly selective functionalization of polymer surfaces. This article reviews the state of the art of surface radical quantification. In addition, a new approach to the generation of radicals on polymer surface is presented. KW - Radikale KW - Polymeralterung KW - Oberflächenanalytik PY - 2005 DO - https://doi.org/10.1002/vipr.200590029 SN - 0947-076X SN - 1522-2454 VL - 17 IS - S1 (Vacuum´s Best) SP - 40 EP - 46 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-13511 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer-Plath, Asmus A1 - Finke, B. A1 - Schröder, K. A1 - Ohl, A. T1 - Pulsed and cw microwave plasma excitation for surface functionalization in nitrogen-containing gases N2 - Results are presented of polymer surface functionalization processes in pulsed and continuous wave (cw) microwave-excited plasmas in nitrogen-containing gases under admixture of hydrogen. A maximum selectivity of 100% for amino groups with respect to all nitrogen functional groups (NH2/N) was obtained in cw microwave (MW) plasmas either for very short treatment durations below 100 µs in pure NH3, or within approximately 10 s in hydrogen-rich nitrogen-containing plasmas. The amino and overall nitrogen surface densities, NH2/C and N/C, reach up to 3.5% and 35%, respectively. Post plasma processes of functionalized polymers are discussed in the light of monofunctionalization. Down to pulse duration of 1 ms, plasma decomposition rates of NH3, determined by infrared absorption spectroscopy, are found to scale linearly with the duty cycle. In this regime, the main effect of a duty cycle variation in pulsed NH3 plasmas on surface functionalization can be interpreted to result from changes in the concentration of the dominant stable species in the gas phase, NH3, N2 and H2, which are activated by subsequent plasma pulses. With increasing duty cycle, NH3 decomposition to N2 and 3H2 more and more dominates over the supply of fresh NH3. The nitrogen-removing role of hydrogen in the plasma is discussed in detail, whereas the role of the numerous transient nitrogen-containing species remains to be studied in the future. KW - Pulsed microwave plasma KW - Amino group KW - Polymer KW - Ammonia KW - Infrared absorption PY - 2003 DO - https://doi.org/10.1016/S0257-8972(03)00563-2 SN - 0257-8972 VL - 174-175 SP - 877 EP - 881 PB - Elsevier Science CY - Lausanne AN - OPUS4-13512 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer-Plath, Asmus A1 - Schröder, K. A1 - Finke, B. A1 - Ohl, A. T1 - Current trends in biomaterial surface functionalization - nitrogen-containing plasma assisted processes with enhanced selectivity N2 - Low-pressure gas-discharge plasmas are widely used for polymer surface functionalization on industrial scale. For biomaterial applications, the density and selectivity of the functionalization are of particular importance, because functional groups control the immobilization of biomolecules. Therefore, surface modification of biomaterials is a challenging task for low-pressure plasma technique. Plasma processes have been successfully applied to various polymer types in order to generate multifunctional surfaces. This paper discusses the present state and the prospects of non-coating plasma processes to generate mono functional surfaces of controlled amino group density. Such surfaces appear most desirable for many applications. The results of various microwave- and radio-frequency- excited plasma processes reported in the literature are reviewed and compared to a sequence of experiments that was conducted in a UHV reaction environment. Non-thermal plasmas are especially well suited for thermally damageable polymers. The effect of hydrogen admixture to discharges in nitrogen and ammonia is discussed in detail. The optimization of process parameters lead to highly selective amino functionalization of high density. The selectivity reached 100% -NH2/N at a surface density of amino groups of 3% -NH2/C. KW - Low pressure plasma KW - Grafting KW - Polymers KW - Amino group KW - Surface analysis PY - 2003 DO - https://doi.org/10.1016/S0042-207X(02)00766-2 SN - 0042-207X VL - 71 IS - 3 SP - 391 EP - 406 PB - Elsevier Science CY - Kidlington AN - OPUS4-13686 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Aminofunktionalisierung mittels Plasmamodifizierung und -polymerisation T2 - 13. Workshop Oberflächentechnologie mit Plasma- und Ionenstrahlprozessen CY - Klingenthal, Germany DA - 2007-03-14 PY - 2007 AN - OPUS4-15348 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Kohlenstoff - Ein altes HiTech-Material mit aufregender Zukunft T2 - BAM-Kolloquium CY - Berlin, Germany DA - 2006-08-23 PY - 2006 AN - OPUS4-15066 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Quantification of nitrogen-containing functional groups on polymer surfaces by merans of chemical derivatization T2 - Polydays 2006 CY - Berlin, Germany DA - 2006-10-04 PY - 2006 AN - OPUS4-15458 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Strategies fot the evaluation of X-ray photoelectron spectroscopy data after chemical derivatization of surface functional groups T2 - 18th International Symposium on Plasma Chemistry CY - Kyoto, Japan DA - 2007-08-28 PY - 2007 AN - OPUS4-15462 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Meyer-Plath, Asmus A1 - Mix, Renate A1 - Friedrich, Jörg Florian ED - Mittal, K. T1 - Aspects of amino functionalization of polypropylene surfaces for adhesion promotion of thermally-evaporated copper films KW - Plasma polymerization KW - Surface functionalization KW - Gas discharge KW - Grafting KW - Amino groups KW - Copper KW - Metallization KW - Adhesion PY - 2007 SN - 978-90-6764-455-6 SN - 90-6764-455-2 VL - 3 SP - 177 EP - 198 PB - VSP CY - Leiden AN - OPUS4-15733 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Selective amino functionalization of polymer surfaces: UV-laser irradiation compared to plasma processing T2 - 18th International Symposium on Plasma Chemistry CY - Kyoto, Japan DA - 2007-08-27 PY - 2007 AN - OPUS4-15759 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Charakterisierung funktionalisierter CNT T2 - Inno.CNT Workshop "Funktionalisierte CNT" CY - Erlangen, Germany DA - 2011-09-20 PY - 2011 AN - OPUS4-24429 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Funktionalisieren von CNT - eine Übersicht über die neuen Möglichkeiten T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25484 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Änderung der elektronischen Eigenschaften von Kohlenstoffnanoröhren durch Funktionalisierung T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25485 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Wettmarshausen, Sascha A1 - Meyer-Plath, Asmus A1 - Ziemann, Sylvia A1 - Hidde, Gundula A1 - Zeynalov, Eldar T1 - Plasmabromierung von graphitischen Materialien - Kovalente Anbindung organischer Moleküle N2 - Die hochselektive und ausbeutereiche plasmachemische Bromierung von Polyolefinoberflächen wurde auf graphitische Materialien übertragen. Oberflächen von graphenartigem Highly Oriented Pyrolytic Graphite (HOPG), natürlichem Graphit, mehrwandige Kohlenstoffnanoröhren (MWCNT) sowie Kohlenstoff-Fasern wurden im Bromdampfplasma behandelt. Während die Bromierung von Polyolefinoberflächen als radikalische Wasserstoffabstraktion mit nachfolgender Addition (Rekombination) oder durch nucleophile Substitution an sp³-hybridisierten C-Atomen abläuft, können graphitische Strukturen sowohl an sp³-hybridisierten Strukturdefekten als auch durch elektrophile Addition an vollständig C-substituierte aromatische Doppelbindungen bromiert werden. Dabei werden die planaren (graphitischen) sp²-C-Atome in die tetraedrische sp³-Hybridisierung umgewandelt und zu elektrisch nichtleitenden Strukturen gefaltet. Die maximalen Bromausbeuten bei Verwendung von Brom als Plasmamedium lagen je nach Substrat zwischen 10–50% Br/C, mit Bromoform deutlich darüber, was durch Kombinationen von Bromoform mit Brom oder Allylbromid mit Bromoform durch Schichtbildung auf über 70% Br/C gesteigert werden konnte. An die C-Br-Gruppen wurden nasschemisch verschiedene Amine nucleophil gepfropft. Die Pfropfausbeuten von 1–10 Moleküle je 100 C lagen deutlich niedriger als die erreichten Pfropfgrade von etwa 1–22 Moleküle je 100 C-Atome an Polyolefinoberflächen. Da nach der chemischen Pfropfung nahezu alle nichtgepfropften Br-Gruppen verschwunden waren, muss auf eine bevorzugte Rekonstruktion der planaren sp²-Graphitschicht geschlossen werden. KW - Polymerbromierung PY - 2012 DO - https://doi.org/10.1002/vipr.201200481 SN - 0947-076X SN - 1522-2454 VL - 24 IS - 1 SP - 24 EP - 29 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-25518 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Harrer, Andrea A1 - Prager, Jens A1 - Kreutzbruck, Marc A1 - Guderian, Matthias A1 - Meyer-Plath, Asmus T1 - Erzeugung von Luftultraschall mit mikro- und nanostrukturierten Kohlenstoffmaterialien unter Ausnutzung des thermoakustischen Prinzips N2 - In diesem Beitrag wird ein neuartiger Ansatz zur Erzeugung von Luftultraschall vorgestellt, der auf dem thermoakustischen Prinzip beruht. Mikro- und nanostrukturierte Kohlenstoffmaterialien werden dabei mit einem harmonischen Wechselstrom gespeist und erfahren durch ohmsche Verluste eine Temperaturänderung, die sich auf das umgebende Fluid überträgt. Daraus resultieren Druckmodulationen, und es wird eine ausbreitungsfähige Schallwelle erzeugt. Dabei tritt Frequenzverdopplung gegenüber der Anregungsfrequenz auf. Es konnte gezeigt werden, dass der entscheidende Parameter für die Effizienz der Methode, d.h. für ein möglichst großes Verhältnis von Schalldruck zu eingebrachter Leistung, die Wärmekapazität pro Flächeneinheit ist. Da dieser Quotient für Kohlenstoffmaterialien sehr klein sein kann, erlaubt das thermoakustische Prinzip hier die effiziente Erzeugung von Luftultraschall. Schalldruckmessungen an verschiedenen Materialproben wurden bis 100 kHz mit einem Mikrofon durchgeführt, oberhalb von 100 kHz wurde eine laservibrometrische Schnellemessung eingesetzt. In experimentellen Untersuchungen wurde die Schallerzeugung in Abhängigkeit der Materialeigenschaften analysiert und systematisiert. Die experimentellen Ergebnisse wurden mit numerischen und analytischen Berechnungsergebnissen verglichen. T2 - DAGA 2011 - 37. Jahrestagung für Akustik - Fortschritte der Akustik CY - Düsseldorf, Germany DA - 21.03.2011 KW - Thermoakustisches Prinzip KW - Luftultraschall KW - Kohelnstoffmaterialien PY - 2011 SN - 978-3-939296-02-7 SP - 339 EP - 340 AN - OPUS4-25328 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - UV-spectroscopic indirekt quantification of functional groups on MWCNTs T2 - Annual World Conference on Carbon 2012 CY - Kraków, Poland DA - 2012-06-17 PY - 2012 AN - OPUS4-26152 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Carbo-Safe - Messung, Feisetzung und Effekte von CNTs T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25447 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Charakterisierung von MWCNT T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25448 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Quantitative chemische Charakterisierung von CNT T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25449 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Plasmaverfahren zur Funktionalisierung und Reinigung von CNT T2 - 4. Jahrestagung inno.CNT CY - Bayreuth, Germany DA - 2012-01-30 PY - 2012 AN - OPUS4-25455 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Daschewski, Maxim A1 - Harrer, Andrea A1 - Prager, Jens A1 - Kreutzbruck, Marc A1 - Guderian, Matthias A1 - Meyer-Plath, Asmus ED - Linde, B. B. J. ED - Paczkowski, J. ED - Ponikwicki, N. T1 - Carbon nanomaterials as broadband airborne ultrasound transducer N2 - A method has been developed for the generation of airborne ultrasound using the thermoacoustic principle applied to carbon materials at the micro- and nanoscale. Such materials are shown to be capable to emitting the ultrasound. We tested the acoustic performance of electrospun polyacrylonitrile-derived carbon nanofibers tissues and determined the sound pressure for frequencies up to 350 kHz. The experimental results are compared to analytic calculations. T2 - International congress on ultrasonics CY - Gdansk, Poland DA - 2011-09-05 KW - Thermoacoustic KW - Airborne ultrasound transducer KW - Sound pressure PY - 2012 SN - 978-0-7354-1019-0 DO - https://doi.org/10.1063/1.3703262 SN - 0094-243X N1 - Serientitel: AIP conference proceedings – Series title: AIP conference proceedings IS - 1433 SP - 624 EP - 627 PB - American Institute of Physics CY - Melville, NY AN - OPUS4-26788 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Ansätze zur quantitativen chemischen Charakterisierung von Kohlenstoffnanoröhren T2 - Fachtagung Nano-Additive CY - Berlin, Germany DA - 2012-11-19 PY - 2012 AN - OPUS4-27167 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Plasmaverfahren zur Funktionalisierung und Reinigung von Kohlenstoffnanoröhren T2 - Fachtagung Nano-Additive CY - Berlin, Germany DA - 2012-11-19 PY - 2012 AN - OPUS4-27168 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Am Ende des Life-Cycle-Assessments von CNT: Freisetzung aus Produkten und Ökotoxizität? T2 - Jahreskongress Innovationsallianz Carbon Nanotubes CY - Fellbach, Germany DA - 2013-02-20 PY - 2013 AN - OPUS4-27889 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Übersicht über die neuen Methoden zur Oberflächenfunktionalisierung T2 - Jahreskongress Innovationsallianz Carbon Nanotubes CY - Fellbach, Germany DA - 2013-02-20 PY - 2013 AN - OPUS4-28028 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Lang, Jacqueline A1 - Meyer-Plath, Asmus T1 - Charakterisierung von nanoskaligen Eigenschaften chemischer Stoffe als Grundlage für die Regulierung im Rahmen der Verordnung (EG) Nr. 1907/2006 (REACH) N2 - Die vorliegende Literaturarbeit zeigt auf, inwiefern die in der Verordnung 440/2008 EG enthaltenen Prüfnachweise für Nanomaterialien anwendbar sind. In einem ersten Teil werden die verschiedenen verwendeten Begriffe für Nanomaterialien erklärt und die Klassifizierung der Nanomaterialien erläutert. Daran schließen sich die Beschreibung der physikalisch-chemischen Eigenschaften von Nanomaterialien und die Charakterisierbarkeit der Nanoskaligkeit mit den in der Verordnung 440/2008 genannten Prüfmethoden an. Im letzten Teil werden die relevanten Eigenschaften von Nanomaterialien aus Sicht internationaler Institutionen beschrieben und die möglichen Bestimmungsmethoden aufgeführt. Abschließend wird analysiert, welche vorhandenen Prüfmethoden der Verordnung 440/2008 auf Nanomaterialien anwendbar sind und welche weiteren Eigenschaften im Rahmen einer Regulierung der Nanomaterialien geprüft werden sollten.---------------------------------------------------------------------------------------------------------------------------------- The presented literature documentation shows the applicability of the test methods listed in regulation EC 440/2008. The first part explains different terms and definitions of nanomaterials and the nanomaterials' classifications. Afterwards the physico-chemical properties of nanomaterials are described and the feasibility to characterise substances at nanoscale with the test methods listed in regulation 440/2008 is assessed. In the last part relevant properties of nanomaterials from the perspective of international institutions are listed and possible methods for the determination are given. Finally, it is analysed which test methods of the regulation EC 440/2008 are applicable to nanomaterials and which further properties should be investigated in the frame of the regulation of nanomaterials. KW - REACH KW - Nanomaterialien KW - Charakterisierung KW - Physikalisch-chemische Daten KW - Nanomaterials KW - Characterisation KW - Physico-chemical data PY - 2012 UR - http://www.baua.de/de/Publikationen/Fachbeitraege/F2261.pdf?__blob=publicationFile&v=3 SP - 1 EP - 112 CY - Dortmund AN - OPUS4-27383 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Bresch, Harald A1 - Meyer-Plath, Asmus A1 - Burgdorf, T. A1 - Packroff, R. A1 - Apel, P. A1 - Adolf, P. A1 - Jesse, A. A1 - Leuschner, C. A1 - Bosse, H. A1 - Dubbert, W. A1 - Epp, A. A1 - Gebel, T. A1 - Götz, M. A1 - Herzberg, F. A1 - Hornbogen, T. A1 - Kersten, N. A1 - Kneuer, C. A1 - Kujath, P. A1 - Pipke, R. A1 - Plitzko, s. A1 - Schlesier, K. A1 - Schröder, F. A1 - Schwirn, K. A1 - Sommer, Y. A1 - Tentschert, J. A1 - Völker, D. A1 - Wolf, T. T1 - 1. Bilanz zur gemeinsamen Forschungsstrategie der Ressortforschungseinrichtungen des Bundes 'Nanotechnologie - Gesundheits- und Umweltrisiken von Nanomaterialien' (2007 - 2011) KW - Nanotechnologie KW - Nanopartikel KW - Nanomaterial KW - Bundesoberbehörden KW - Forschungsstrategie PY - 2013 SP - 1 EP - 124 CY - Berlin AN - OPUS4-28538 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zeynalov, Eldar A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus A1 - Hidde, Gundula A1 - Nuriyev, L. A1 - Aliyeva, A. Z. A1 - Cherepnova, Y. T1 - Plasma-chemically brominated single-walled carbon nanotubes as novel catalysts for oil hydrocarbons aerobic oxidation N2 - Brominated single-walled carbon nanotubes [(Br)n-SWCNT) produced by the plasma-chemical technique were involved in the liquid-phase process of hydrocarbons aerobic oxidation. The significant catalytic effect of the (Br)n-SWCNT was revealed at first by the cumene initiated model oxidation and then in experiments on profound aerobic oxidation of petroleum naphthenic fraction derived from the commercial Azerbaijan (Baku) oils blend diesel cut. The ability of (Br)n-SWCNT to accelerate the aerobic oxidation of the hydrocarbons was found out for the first time. Obviously this phenomenon originates from the peculiarities of electronic configuration of the (Br)n-CNT patterns. The plausible mechanism of (Br)n-SWCNT catalytic action is inclined to the formation of reactive oxygen species. The catalytic activity of (Br)n-SWCNT markedly exceeds the activity of the industrial catalysts, manganese salt of indigenous petroleum acids, used for the liquid phase petroleum hydrocarbons oxidation process. KW - Brominated carbon nanotubes KW - Plasma-chemical technique KW - Model cumene oxidation KW - Oxidation rate KW - Oxidation catalysts KW - Oil hydrocarbons liquid-phase oxidation KW - Manganese naphthenate KW - Synthetic petroleum acids PY - 2013 DO - https://doi.org/10.1016/j.apcata.2013.01.003 SN - 0926-860X SN - 1873-3875 VL - 454 SP - 115 EP - 118 PB - Elsevier CY - Amsterdam AN - OPUS4-28290 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schröder, K. A1 - Meyer-Plath, Asmus A1 - Keller, D. A1 - Ohl, A. T1 - On the Applicability of Plasma Assisted Chemical Micropatterning to Different Polymeric Biomaterials N2 - A plasma process sequence has been developed to prepare chemical micropatterns on polymeric biomaterial surfaces. These patterns induce a guided localized cell layover at microscopic dimension. Two subsequent plasma steps are applied. In the first functionalization step a microwave ammonia plasma introduces amino groups to obtain areas for very good cell adhesion; the second passivation step combines pattern generation and creation of cell repelling areas. This downstream microwave hydrogen plasma process removes functional groups and changes the linkages of polymer chains at the outermost surfaces. Similar results have been obtained on different polymers including polystyrene (PS), polyhydroxyethylmethacrylate (PHEMA), polyetheretherketone (PEEK), polyethyleneterephthalate (PET) and polyethylenenaphthalate (PEN). Such a rather universal chemical structuring process could widen the availability of biomaterials with specific surface preparations. KW - Microwave plasma KW - Ammonia KW - Hydrogen KW - Polymer surface KW - Cell culture KW - XPS KW - Fluorescence PY - 2002 DO - https://doi.org/10.1023/A:1016239302194 SN - 1084-0184 SN - 1572-8978 VL - 7 IS - 2 SP - 103 EP - 125 PB - Plenum Press CY - New York, NY AN - OPUS4-1729 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Barthel, Anne-Kathrin A1 - Wachtendorf, Volker A1 - Sturm, Heinz A1 - Meyer-Plath, Asmus ED - Reichert, T. T1 - Irradiation-induced surface changes on CNT-filled polymeric materials N2 - The present study examines weathering-related degradation mechanisms of CNT-containing polymers and discusses whether and under what conditions degradation might lead to the release of nanoscale components. For this purpose, the study used accelerated artificial aging. The photodegradation of composites based polycarbonate containing multi-walled CNTs of type "Baytubes C150P" was studied under irradiation with a Xenon-arc irradiation device (λ-cut-off at 290 nm). Resulting surface modifications were evaluated with complementary chemical and microscopic characterization techniques. At sufficiently high radiation dose, a significant degradation of the matrix was observed for some of the polymers under examination which led to entangled networks of uncovered CNT at the composite surface. By investigation of potential exposure mechanisms of CNTs in polymer composites, the present work contributes to the risk assessment of CNT-containing products. T2 - 6th European weathering symposium Natural and artificial ageing of polymers CY - Bratislava, Slovak Republic DA - 11.09.2013 PY - 2013 SN - 978-3-9813136-8-0 N1 - Serientitel: CEEES Publication – Series title: CEEES Publication IS - 16 SP - 295 EP - 308 AN - OPUS4-31161 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - High-power airborne ultrasound emitters - Structural optimization of carbon-based fibrous materials T2 - 14th International Conference on the Science and Application of Nanotubes (NT13) CY - Helsinki, Finland DA - 2013-06-24 PY - 2013 AN - OPUS4-28474 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer-Plath, Asmus A1 - Beckert, F A1 - Tölle, FJ A1 - Sturm, Heinz A1 - Mülhaupt, R T1 - Stable aqueous dispersions of functionalized multi-layer graphene by pulsed underwater plasma exfoliation of graphite N2 - A process was developed for graphite particle exfoliation in water to stably dispersed multi-layer graphene. It uses electrohydraulic shockwaves and the functionalizing effect of solution plasma discharges in water. The discharges were excited by 100 ns high voltage pulsing of graphite particle chains that bridge an electrode gap. The underwater discharges allow simultaneous exfoliation and chemical functionalization of graphite particles to partially oxidized multi-layer graphene. Exfoliation is caused by shockwaves that result from rapid evaporation of carbon and water to plasma-excited gas species. Depending on discharge energy and locus of ignition, the shockwaves cause stirring, erosion, exfoliation and/or expansion of graphite flakes. The process was optimized to produce long-term stable aqueous dispersions of multi-layer graphene from graphite in a single process step without requiring addition of intercalants, surfactants, binders or special solvents. A setup was developed that allows continuous production of aqueous dispersions of flake size-selected multi-layer graphenes. Due to the well-preserved sp(2)-carbon structure, thin films made from the dispersed graphene exhibited high electrical conductivity. Underwater plasma discharge processing exhibits high innovation potential for morphological and chemical modifications of carbonaceous materials and surfaces, especially for the generation of stable dispersions of two-dimensional, layered materials. KW - Exfoliation KW - Graphene KW - Aqueous dispersion KW - Solution plasma KW - Functionalization KW - Electrohydraulic effect KW - Shear exfoliation KW - Oxide-films KW - Water PY - 2016 DO - https://doi.org/10.1088/0022-3727/49/4/045301 SN - 0022-3727 VL - 49 IS - 4 SP - 045301-1 EP - 045301-11 AN - OPUS4-35796 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - CarboLifeCycle - CNT Materials: Properties, Release, Fate and Effects in the Environment T2 - Inno. CNT Jahrestagung CY - Ettlingen, Germany DA - 2011-01-25 PY - 2011 AN - OPUS4-23095 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer-Plath, Asmus A1 - Orts Gil, Guillermo A1 - Petrov, Sergej A1 - Oleszak, Franz A1 - Maneck, Heinz-Eberhard A1 - Dörfel, Ilona A1 - Haase, Oskar A1 - Richter, Silke A1 - Mach, Reinhard T1 - Plasma-thermal purification and annealing of carbon nanotubes N2 - We have developed a very fast and entirely gas-phase based purification technique for carbon nanotubes (CNT) that allows removing metal and metal oxide impurities with high effectiveness. CNT agglomerates from chemical vapor deposition (CVD) synthesis which contained carbon encapsulated catalysts were injected into an atmospheric plasma torch. Very high heating rates allow for quasi-instantaneous vaporization of catalyst particles. This way, metal vapors are hyposized to break mechanically instable encapsulations and effuse from incomplete ones faster than thermally induced graphitization stabilizes such particle encapsulations. The ash content of multi-walled (MW) CNT samples was reduced to less than 15% of the initial value within a few milliseconds. Also the metal content of single-walled (SW) CNT agglomerates was significantly reduced. Repeated injection of CNT agglomerates into the plasma torch resulted in higher-purity products of improved structural integrity and increased oxidation resistance. PY - 2012 DO - https://doi.org/10.1016/j.carbon.2012.04.049 SN - 0008-6223 SN - 1873-3891 VL - 50 IS - 10 SP - 3934 EP - 3942 PB - Pergamon Press CY - New York, NY AN - OPUS4-25986 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Irradiation-induced surface changes of CNT-containing polymer-based nanocomposites T2 - 14th International Conference on the Sience and Application of Nanotubes (NT13) CY - Helsinki, Finland DA - 2013-06-24 PY - 2013 AN - OPUS4-28475 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Meyer-Plath, Asmus T1 - Bestrahlungsinduzierte Oberflächenveränderungen CNT-gefüllter Polymerwerkstoffe T2 - Jahreskongress Innovatioinsallianz Carbon Nanotubes CY - Fellbach, Germany DA - 2013-02-20 PY - 2013 AN - OPUS4-27888 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hanelt, Sven A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus T1 - UV spectrometric indirect analysis of brominated MWCNTs with UV active thiols and an alkene-reaction kinetics, quantification and differentiation of adsorbed bromine and oxygen N2 - Indirect UV-absorption spectrometry was shown to be a valuable tool for chemical characterization of functionalized carbon nanotubes (CNTs). It complements data from X-ray photoelectron spectroscopy (XPS) or FTIR analysis since it helps to clarify the type and concentration of functional groups. The principles of indirect application of UV-spectrometry and its mathematical interpretation are discussed. Their facile application, together with their adequate sensitivity and high flexibility, make UV-absorption-based approaches a valuable alternative to fluorescence spectrometry. Here, the approach was applied to the chemical analysis of oxidizing substances on CNTs. For this, pristine CNTs of low but finite oxygen content as well as brominated CNTs were analyzed by reaction in suspension with UV-active thiol reagents and a styrene derivative. It was shown that carefully selected reagents allow differentiation and quantification of bromine and generally oxidizing entities like oxygen. For brominated CNTs, it was shown that physisorbed bromine may dominate the overall bromine content. KW - Carbon nanotubes KW - CNTs KW - UV-spectrometry KW - Bromination KW - Thiols KW - Mercaptans KW - Disulfides KW - Quantification KW - Kinetics PY - 2013 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-289077 DO - https://doi.org/10.3390/ma6083035 SN - 1996-1944 VL - 6 IS - 8 SP - 3035 EP - 3063 PB - MDPI CY - Basel AN - OPUS4-28907 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Anik, Yavuz A1 - Geburtig, Anja A1 - Sturm, Heinz A1 - Meyer-Plath, Asmus ED - Reichert, T. T1 - CarboLifeCycle -weathering-induced degradation of nanoparticle-functionalised composites N2 - A new research project 'CarboLifeCycle', funded by the German Federal Ministry of Education and Research (BMBF), investigates various nanoparticle release scenarios for carbon nanotube-containing polymer composites. The studied weathering concepts and conditions will be described. T2 - 5th European weathering symposium - Natural and artificial ageing of polymers CY - Lisbon, Portugal DA - 21.09.2011 KW - CNT KW - Nanoparticle KW - Weathering KW - Degradation PY - 2011 SN - 978-3-9813136-2-8 N1 - Serientitel: CEEES Publication – Series title: CEEES Publication IS - 15 SP - 125 EP - 135 PB - GUS (Gesellschaft für Umweltsimulation) CY - Pfinztal AN - OPUS4-24503 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Harrer, Andrea A1 - Daschewski, Maxim A1 - Prager, Jens A1 - Kreutzbruck, Marc A1 - Guderian, Matthias A1 - Meyer-Plath, Asmus T1 - Thermoacoustic generation of airborne ultrasound using carbon materials at the micro- and nanoscale N2 - The generation of airborne ultrasound is presented using the thermoacoustic principle applied to carbon materials at the micro- and nanoscale. Such materials are shown to be capable of emitting ultrasound when being fed by an alternating current. We tested the acoustic performance of carbon fibers, bucky papers and electrospun polyacrylonitrile-derived carbon nanofibers and determined the sound pressure for frequencies up to 350 kHz. A comparison between the experimental results and the theoretical prediction showed remarkable agreement for frequencies up to 150 kHz. Beyond 150 kHz, we found slight deviations from the expected sound pressure dependence on the square root of the frequency. KW - Thermoacoustic KW - Airborne ultrasound transducer KW - Sound pressure PY - 2012 DO - https://doi.org/10.3233/JAE-2012-1440 SN - 1383-5416 SN - 0925-2096 VL - 39 IS - 1-4 SP - 35 EP - 41 PB - IOS Press CY - Amsterdam, The Netherlands AN - OPUS4-26737 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hanelt, Sven A1 - Friedrich, Jörg Florian A1 - Orts Gil, Guillermo A1 - Meyer-Plath, Asmus T1 - Study of Lewis acid catalyzed chemical bromination and bromoalkylation of multi-walled carbon nanotubes N2 - Chemical functionalization of carbon nanotubes (CNT) with nucleophiles requires introduction of electrophilic reactive sites on the CNTs. This can, for instance, be accomplished by the chemical bromination procedure with elemental bromine and a set of Lewis acids (BBr3, BF3 × Et2O, AlBr3, FeBr3, ZnBr2, TiBr4, SiBr4, SnBr4, VBr3) or a radical starter like dibenzoylperoxide (DBPO) in appropriate solvents at varied temperature. The present approach to electrophilic sites relies on the well-known electrophilic aromatic substitution or addition of bromine with aromatic structural units. In addition to the use of bromine, the introduction of haloalkyl groups was also investigated here using bis-electrophiles or haloalcohols and Brønsted acids. The advantages and drawbacks of the studied reaction conditions, the obtained degree of bromination as analyzed by X-ray photoelectron spectroscopy (XPS) and the amount of introduced bromine that can be substituted by a nucleophile are presented and discussed. KW - Carbon nanotubes KW - Bromierung KW - Lewis Säure KW - Bromalkylierung KW - CNT PY - 2012 DO - https://doi.org/10.1016/j.carbon.2011.11.009 SN - 0008-6223 SN - 1873-3891 VL - 50 IS - 3 SP - 1373 EP - 1385 PB - Pergamon Press CY - New York, NY AN - OPUS4-25207 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wettmarshausen, Sascha A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus A1 - Kalinka, Gerhard A1 - Hidde, Gundula A1 - Weidner, Steffen T1 - Coating of carbon fibers with adhesion-promoting thin poly(acrylic acid) and poly(hydroxyethylmethacrylate) layers using electrospray ionization N2 - Thin coatings of poly(acrylic acid) (PAA) and poly(hydroxyethylmethacrylate) (PHEMA) were deposited onto carbon fibers by means of the electrospray ionization (ESI) technique in ambient air. These high-molecular weight polymer layers were used as adhesion promoters in carbon fiber–epoxy resin composites. Within the ESI process, the carbon fibers were completely enwrapped with polymer in the upper 10 plies of a carbon fiber roving. As identified with scanning electron microscopy also shadowed fibers in a bundle as well as backsides of fiber rovings were pinhole-free coated with polymers (‘electrophoretic effect'). Under the conditions used, the layers have a granular structure. Residual solvent was absent in the deposit. PAA and PHEMA films did not show any changes in composition and structure in comparison with the original polymers as analyzed by X-ray photo-electron spectroscopy and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Single-fiber pullout tests of coated fibers embedded in epoxy resin showed significantly increased interfacial shear strength. It is assumed that chemical bonds between carbon fiber poly(acrylic acid) and epoxy resin contribute significantly to the improved interactions. KW - Adhesion promotion KW - Thin polymer layers KW - Electrospray ionization (ESI) KW - Carbon fiber–epoxy resin laminates KW - Layer topography PY - 2015 DO - https://doi.org/10.1080/01694243.2015.1040980 SN - 0169-4243 SN - 1568-5616 VL - 29 IS - 15 SP - 1628 EP - 1650 PB - VNU Science Press CY - Utrecht AN - OPUS4-34564 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -