TY - CONF A1 - Friedrich, Jörg Florian T1 - Study of Metal-Polymer Interfaces: Relevance to Adhesion T2 - ACS spring meeting CY - Boston, MA, USA DA - 2010-08-21 PY - 2010 AN - OPUS4-22738 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Erfahrungsaustaussch: Oberflächentechnologie mit Plasma- und Ionenstrahlprozessen T2 - Vortrag CY - Klingenthal, Germany DA - 2010-03-02 PY - 2010 AN - OPUS4-22739 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 - JOUR A1 - Friedrich, Jörg Florian A1 - Wettmarshausen, Sascha A1 - Hennecke, Manfred T1 - Haloform plasma modification of polyolefin surfaces N2 - Polyolefin surfaces (polyethylene and polypropylene) were exposed to haloform (CHX3) plasmas for introduction of monosort halogen groups. Bromoform and chloroform plasmas produced selectively C-Br (100 Br/100 C) and C-Cl (200 Cl/100 C) groups in high yields. The bromoform plasma showed 1-3 and the chloroform plasma 2-7 post-plasma introduced O-functionalities per 100 C. The polyolefin C-Br groups were grafted wet-chemically or by exposure to the vapour of amines, diols and glycols. Thus, spacer molecules could be covalently bonded to maximal 15 spacer molecules per 100 C for the smallest grafted molecules and 1.2 molecules/100 C for larger molecules as octaaminophenylene-POSS. After metal evaporation the end groups of these polymer-bonded spacer molecules formed also covalent bonds to the metal. Thus, flexible, hydrophobic and barrier elements were introduced into the polymer-metal interfaces for high-impact, high-durable and water-resistant metal-polymer composites as measured by means of peel strengths. KW - Bromination KW - Chlorination KW - Selective plasma processes KW - Spacer grafting PY - 2009 DO - https://doi.org/10.1016/j.surfcoat.2009.05.050 SN - 0257-8972 VL - 203 IS - 23 SP - 3647 EP - 3655 PB - Elsevier Science CY - Lausanne AN - OPUS4-23204 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Friedrich, Jörg Florian ED - Blasek, G. ED - Bräuer, G. T1 - Modifizieren und Beschichten von Polymeroberflächen KW - Plasma-Oberflächenreinigung PY - 2010 SN - 978-3-87480-257-4 IS - Kap. 2.6 SP - 537 EP - 601 ff. PB - Eugen G. Leuze CY - Bad Saulgau AN - OPUS4-23275 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Friedrich, Jörg Florian A1 - Krüger, P. ED - Blasek, G. ED - Bräuer, G. T1 - Feinreinigung von Oberflächen mit Niederdruckplasmen KW - Plasma-Oberflächenreinigung PY - 2010 SN - 978-3-87480-257-4 IS - Kap. 3.15 SP - 1085 EP - 1106 PB - Eugen G. Leuze CY - Bad Saulgau AN - OPUS4-23273 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Friedrich, Jörg Florian ED - Blasek, G. ED - Bräuer, G. T1 - Plasmapolymerisation KW - Plasma-Oberflächenreinigung PY - 2010 SN - 978-3-87480-257-4 IS - Kap. 2.4 SP - 356 EP - 451 PB - Eugen G. Leuze CY - Bad Saulgau AN - OPUS4-23274 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fahmy, A. A1 - Mix, Renate A1 - Schönhals, Andreas A1 - Friedrich, Jörg Florian T1 - Structure of plasma-deposited poly(acrylic acid) films N2 - Poly(acrylic acid) films with a thickness of about 150?nm were deposited using a pulsed plasma onto aluminum and glass. The structure/property relationships of these samples were studied in dependence to the duty cycle (DC) of the plasma by a broad combination of different techniques and probes. For the first time, volume sensitive methods (FTIR, dielectric spectroscopy, and differential scanning calorimetry) are combined with surface analyses i.e. XPS. For an unambiguous identification of COOH groups by XPS, derivatization with trifluoroethanol was accomplished. Quantitative FTIR investigations give qualitatively a dependence of the concentration of COOH groups upon DC similar to that given by XPS investigations. The observed differences are discussed considering the different analytical depths of both methods. The dielectric measurements reveal that the structure of the plasma deposited films is different from that of the bulk material. Moreover, these measurements show also that the plasma deposited films are not thermally stable but undergo a post plasma chemical reaction during heating, where the reaction kinetics depends on DC. PY - 2011 DO - https://doi.org/10.1002/ppap.201000108 SN - 1612-8850 SN - 1612-8869 VL - 8 IS - 2 SP - 147 EP - 159 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-23478 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fahmy, A. A1 - Mix, Renate A1 - Schönhals, Andreas A1 - Friedrich, Jörg Florian T1 - Structure-property relationship of thin plasma deposited poly(allyl alcohol) films N2 - Poly(allyl alcohol) films with a thickness of about 150 nm were deposited by pulse plasma polymerization onto different substrates (inorganic and organic). The structure/property relationships of these samples were studied in dependence on the duty cycle (DC) of the plasma by a broad combination of different techniques and probes. For the first time volume sensitive methods (FTIR and dielectric spectroscopy) are combined with surface analytics by employing XPS for that system. FTIR spectroscopy gives qualitatively the same dependence of the concentration of the OH groups on DC like XPS. The observed differences are discussed considering the different analytical depths of both the methods. The dielectric measurements show that the plasma deposited films are not thermally stable but undergo a post plasma chemical reaction during heating. The results obtained by dielectric spectroscopy are discussed in detail with the data from FTIR and XPS measurements. KW - Allyl alcohol KW - Dielectric properties KW - Plasma polymerization KW - Surface and bulk characterization KW - Thermal stability PY - 2011 DO - https://doi.org/10.1007/s11090-011-9297-0 SN - 0272-4324 VL - 31 IS - 3 SP - 477 EP - 498 PB - Plenum Publ. Corp. CY - New York, NY, USA AN - OPUS4-23671 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Min, Hyegeun A1 - Wettmarshausen, Sascha A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang T1 - A ToF-SIMS study of the deuterium-hydrogen exchange induced by ammonia plasma treatment of polyolefins N2 - ToF-SIMS has been used to study the surface functionalization of polypropylene and polyethylene samples by exposure to low-pressure ammonia plasma. Static secondary ion mass spectrometry is an appropriate tool to determine hydrogen isotopes as elements and in fragment ions with high sensitivity and selectivity. Specifically the exchange of hydrogen isotopes and the incorporation of N-containing moieties in the near-surface layer of the polyolefins have been studied in ND3 plasma experiments with conventional polypropylene (h-PP) and polyethylene (h-PE) and NH3 plasma experiments with deuterated polyethylene (d-PE). Considering the exchange of hydrogen between the plasma and the polymer surface studied by using deuterated ammonia and polyolefin samples the conclusion has been derived that polypropylene with its side chain methyl groups is more susceptible to hydrogen exchange reactions. For ND3 plasma treatment of polyethylene and polypropylene similar N-containing fragments were obtained and the measured semi-quantitative ToF-SIMS N-uptake data are rather similar. The observation of a wide range of characteristic mixed CkNlHmDn+ secondary fragment ions suggests complex and manifold reaction pathways at the polymer–plasma interface besides simple grafting of –ND2 or –NH2 moieties formed by ammonia fragmentation in the plasma. Finally, indications of an isotopic effect for hydrogen isotopes in the plasma process have been observed by comparison of ND3/h-PE results with those of NH3/d-PE. KW - ToF-SIMS KW - Hydrogen-deuterium exchange KW - Ammonia plasma treatment KW - Amine-functionalized polymer KW - Polyolefins PY - 2011 DO - https://doi.org/10.1039/c1ja10043b SN - 0267-9477 SN - 1364-5544 VL - 26 SP - 1157 EP - 1165 PB - Royal Society of Chemistry CY - London AN - OPUS4-23754 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -