TY - JOUR A1 - Friedrich, Jörg Florian A1 - Hidde, Gundula A1 - Lippitz, Andreas A1 - Unger, Wolfgang T1 - Plasma bromination of graphene for covalent bonding of organic molecules N2 - Plasma-chemical bromination applied to graphitic materials, in particular to highly ordered pyrolytic graphite is reviewed. The resulting bromination efficiency of the plasma-chemical treatment was subject of systematic process optimization. The plasma of elemental bromine vapour produced bromine concentrations on graphene surfaces of more than 30 % Br/C using either inductively or capacitively coupled low-pressure radio-frequency plasmas. Plasma brominated graphite surfaces have been studied by Near Edge X-ray Absorption Fine Structure, X-ray Photoelectron Spectroscopy, Atomic Force Microscopy and Scanning Electron Microscopy. The introduction of bromine into graphene-like graphite layers and its binding situation were investigated. To study the physical effect of the plasma bromination process, Kr plasma was also used because of its chemical inertness but similar atomic mass. Covering the samples with a Faraday cage or with a LiF window should help to differentiate between physical, chemical and radiation effects of the plasma. Bromination was assigned to radical or electrophilic addition of bromine onto fully substituted aromatic double bonds (sp² C) with exothermal reaction enthalpy. Low bromination shows a strong decay of aromatic double bonds, higher bromination percentage let disappear all aromatic rings. The formed C–Br bonds were well suited for efficient grafting of organic molecules by post-plasma wet-chemical nucleophilic substitution. This grafting onto the graphene surface was demonstrated using aminosilane and different diamines. The bromination of double bonds changes the hybridization of carbon atoms from plane sp² to tetrahedral sp³ hybridization. Thus, the plane topography of graphene is destroyed and the conductivity is lost. KW - Graphene KW - Bromination KW - Grafting of diamines KW - Plasma KW - Organic graphting PY - 2014 DO - https://doi.org/10.1007/s11090-013-9509-x SN - 0272-4324 VL - 34 SP - 621 EP - 645 PB - Plenum Publ. Corp. CY - New York, NY, USA AN - OPUS4-30575 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian ED - Gutowski, W. ED - Dodiuk, H. T1 - Study of metal-polymer interfaces: Relevance to adhesion KW - Polymer surface modification KW - Adhesion KW - Spacer PY - 2013 SN - 978-90-04-20173-6 SN - 978-90-04-20174-3 SP - 3 EP - 33 PB - CRC Press AN - OPUS4-30576 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Heise, C. A1 - Schedler, U. A1 - Wettmarshausen, Sascha A1 - Friedrich, Jörg Florian T1 - Plasma-brominated cyclo-olefin polymer slides: Suiitable macroinitiators for activator regenerated by electron transfer/atom radical transfer polymerization N2 - Activators regenerated by electron transfer–atom radical transfer polymerization (ATRP) as a controlled living polymerization are distinguished by their acceptance of small amounts of transition-metal complexes and oxygen and by their tolerance of reducing agents at a high concentration. The precondition of all ATRP applications is the use of homolytic or heterolytic cleavable halides as a dormant species; this allows the propagation of monomer chains. Hence, alkyl bromides are slightly cleavable and are the preferred initiators for ATRP. The bromination of polymer slides used as macroinitiators was carried out under gentle bromoform plasma conditions. This led to an oxidation-resistant stable bromine layer. More than 20 bromines per 100 carbons on the polymer scaffold were permanently bound to the substrate after plasma treatment. The resulting amounts of secondary and tertiary bromines on the polymer scaffold exhibited a suitable macroinitiator concentration for the surface-initiated polymerization of methyl methacrylate and glycidyl methacrylate. KW - Copolymers KW - Functionalization of polymers KW - Grafting KW - Monolayers and polymer brushes KW - Radical polymerization PY - 2014 UR - http://onlinelibrary.wiley.com/doi/10.1002/app.40662/full DO - https://doi.org/10.1002/APP.40662 SN - 0021-8995 SN - 1097-4628 VL - 131 IS - 16 SP - 40662-1 EP - 40662-10 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-30577 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Natte, Kishore A1 - Friedrich, Jörg Florian A1 - Wohlrab, Sebastian A1 - Lutzki, J. A1 - von Klitzing, R. A1 - Österle, Werner A1 - Orts-Gil, Guillermo T1 - Impact of polymer shell on the formation and time evolution of nanoparticle-protein corona N2 - The study of protein corona formation on nanoparticles (NPs) represents an actual main issue in colloidal, biomedical and toxicological sciences. However, little is known about the influence of polymer shells on the formation and time evolution of protein corona onto functionalized NPs. Therefore, silicapoly(ethylene glycol) core–shell nanohybrids (SNPs@PEG) with different polymer molecular weights (MW) were synthesized and exhaustively characterized. Bovine serum albumin (BSA) at different concentrations (0.1–6 wt%) was used as model protein to study protein corona formation and time evolution. For pristine SNPs and SNPs@PEG (MW = 350 g/mol), zeta potential at different incubation times show a dynamical evolution of the nanoparticle–protein corona. Oppositely, for SNPs@PEG with MW ≥2000 g/mol a significant suppression of corona formation and time evolution was observed. Furthermore, AFM investigations suggest a different orientation (side-chain or perpendicular) and Penetration depth of BSA toward PEGylated surfaces depending on the polymer length which may explain differences in protein corona evolution. KW - Nanoparticles KW - Silica KW - PEGylation KW - Protein corona KW - BSA KW - Biointerface PY - 2013 DO - https://doi.org/10.1016/j.colsurfb.2012.11.019 SN - 0927-7765 VL - 104 SP - 213 EP - 220 PB - Elsevier AN - OPUS4-38547 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Natte, Kishore A1 - Österle, Werner A1 - Friedrich, Jörg Florian A1 - von Klitzing, R. A1 - Orts-Gil, Guillermo T1 - Tuning interfacial properties and colloidal behavior of hybrid nanoparticles by controlling the polymer precursor N2 - A facile and versatile synthetic route for controlling the size and surface potential of organic–inorganic hybrid silica nanoparticles (NPs) is introduced in this paper. For polymer-grafted NPs, the density of polymer chains on the surface is strongly affected by the concentration of precursor. Nevertheless, for condensed NPs, the precursor concentration determines the particle size but not the density of polymer chains on the surface or the adsorption of bovine serum albumin (BSA). Results presented here may have Major implications in biomedical and colloidal chemistry since interfacial and colloidal properties are known to drive several processes associated with nanoparticles in biological media. KW - BSA KW - Bio-interface KW - Nanosilica hybrids KW - PEG KW - Protein corona PY - 2012 DO - https://doi.org/10.1002/macp.201200148 SN - 0025-116X SN - 1022-1352 SN - 1521-3935 VL - 213 IS - 22 SP - 2412 EP - 2419 PB - Whiley-VCH CY - Weinheim AN - OPUS4-38549 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Farag, Zeinab A1 - Moustapha, M. A1 - Hidde, Gundula A1 - Friedrich, Jörg A1 - Azzam, M. A1 - Krüger, Simone ED - Mital, K.L. T1 - Promotion of Adhesion of Green Flame Retardant Coatings onto Polyolefins by Depositing Ultra-Thin Plasma Polymer Films N2 - Various methods have been used for introducing fire retardant additives into polymers. Deposition of thick fire retardant coatings directly onto polymer substrates is an alternative technique. An important advantage of the coating technique is the preservation of the physical and chemical integrity of the polymer material. Moreover, the fire retardancy of the polymer materials can be achieved following their production. Suitable coating materials are inorganics, intumescent, char-forming, oxygendiluting, and cooling or radical quenching layers. The most important problem is to achieve sufficient coating thickness to withstand the direct attack of flame and to protect the polymer bulk from pyrolysis, otherwise blistering of coating, caused by emitted pyrolysis gases, is often observed. To avoid blistering of coating, the adhesion between polyolefin substrate and fire retardant coating has to be extraordinarily high. In order to achieve such a high level of adhesion, the polymer surface has to be modified with adhesion-promoting functional groups. The deposition of thin plasma polymers as adhesion-promoting layers with NH2, OH or COOH groups has been the most suited method. These functional groups are able to form covalent bonds and other interactions between the fire-resistant coating and the plasma-modified polyolefin substrate. Additionally, the plasma polymer counteracts the strong mechanical stresses in the laminate on exposure to high temperatures by its flexibility. KW - Plasma KW - Adhesion PY - 2017 SN - 978-1-119-40748-5 SN - 978-1-119-40638-9 DO - https://doi.org/10.1002/9781119407485 VL - 2 SP - 399 EP - 427 PB - Scrivener Publishing CY - Beverly, USA AN - OPUS4-47227 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Simone A1 - Friedrich, Jörg A1 - Hidde, Gundula A1 - Farag, Zeinab R. A1 - Moustapha, Moustapha E. A1 - Azzam, Maged M. T1 - Promotion of adhesion of green flame retardant coatings onto polyolefins by depositing ultra-thin plasma polymer films: A critical review N2 - Various methods have been used for introducing fire retardant additives into polymers. Deposition of thick fire retardant coatings directly onto polymer substrates is an alternative technique. An important Advantage of the coating technique is the preservation of the physical and chemical integrity of the polymer material. Moreover, the fire retardancy of the polymer materials can be achieved following their production. Suitable coating materials are inorganics, intumescent, char-forming, oxygendiluting, and cooling or radical quenching layers. The most important problem is to achieve sufficient coating thickness to withstand the direct attack of flame and to protect the polymer bulk from pyrolysis, otherwise blistering of coating, caused by emitted pyrolysis gases, is often observed. To avoid blistering of coating, the adhesion between polyolefin Substrate and fire retardant coating has to be extraordinarily high. In order to achieve such a high level of adhesion, the polymer surface has to be modified with adhesion-promoting functional groups. The deposition of thin plasma polymers as adhesion-promoting layers with NH2, OH or COOH groups has been the most suited method. These functional groups are able to form covalent bonds and other interactions between the fire-resistant coating and the plasma-modified polyolefin substrate. Additionally, the plasma polymer counteracts the strong mechanical stresses in the laminate on exposure to high temperatures by its flexibility. The thick fire retardant coatings were chosen based on “green” ecological aspects to avoid flame-initiated emission of toxic or corrosive gases and remains of toxic char. KW - Flame retardant KW - Adhesion KW - Coating PY - 2016 DO - https://doi.org/10.7569/RAA.2016.097314 SN - 2168-0965 SN - 2168-0973 VL - 4 IS - 4 SP - 417 EP - 447 PB - Scrivener Publishing LLC AN - OPUS4-48164 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zeynalov, Eldar A1 - Maherramova, S.N. A1 - Sadieva, N.F. A1 - Iskenderova, S.A. A1 - Agayev, B. K. A1 - Friedrich, Jörg Florian T1 - New softeners for polyvinylchloride N2 - Die Produktion von neuen effektiven und 'grünen' Weichmachern für Polyvinylchlorid (PVC) stellt eine der großen Herausforderungen in der chemischen Industrie dar. In diesem Beitrag wird über Ergebnisse von Untersuchungen berichtet, in denen symmetrische Ester einer Reihe von Fettsäuren und Triethylenglykol (TEG) gewonnen wurden und die als effektive Plastifizierungskomponenten verwendet wurden. Die Veresterung wurde unter Zugabe von Titandioxid Degussa P-25 in Nanopartikelgröße als umweltverträgliche Technologie durchgeführt. Eine gute Verträglichkeit und eine niedrige Flüchtigkeit der Ester auf Biobasis in den PVC-Rezepturen werden gezeigt und es konnten bessere physiko-mechanische Eigenschaften der PVC-Komposite eingestellt werden. Die Ester können als effektive und umweltfreundliche PVC-Weichmacher und als Ersatz für herkömmliche Phtalate empfohlen werden. N2 - Production of new types of effective and green softeners for polyvinylchloride (PVC) is one of the important concerns in chemical industry. The paper reports results of investigations on obtaining symmetric esters of a series of fatty acids and triethylene glycol (TEG) and their use as effective PVC plasticizing agents. The esterification process was conducted in the presence of nano-grade titanium dioxide Degussa P-25 and specified by environmentally sound technology. Good compatibility and low volatility of the bio-based type esters in PVC formulations were shown and higher physico-mechanical features of the PVC composites were established. The esters may be recommended as effective and environmentally friendly PVC softeners to replace commonly used phthalates. KW - Softener KW - Polyvinylchloride PY - 2012 SN - 0025-5300 VL - 54 IS - 4 SP - 246 EP - 248 PB - Hanser CY - München AN - OPUS4-25747 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mohamed, Zeinab A1 - Friedrich, Jörg Florian A1 - Krüger, Simone A1 - Farouk, M. A1 - Moustapha, M.E. T1 - Plasma deposition of adhesion-promoting polymer layers onto polypropylene for subsequent covering with thick fire retardant coatings N2 - Melamine resins were used as 50-µm-thick fire retardant coatings for polypropylene (PP). Preceding deposition, low-pressure plasma polymer films of allyl alcohol were coated onto PP to improve the adhesion between PP and melamine resin coatings. The efficiency of such fire retardant coatings was confirmed by flame tests. The plasma-deposited polymer and the dip-coated melamine resin films were characterized by Fourier transform infrared-attenuated total reflectance spectroscopy and X-ray photoelectron spectroscopy (XPS). The adhesion of coatings was measured using a 90° peel test with a doubled-faced adhesive tape. To detect the locus of failure, the peeled layer surfaces were inspected using optical microscopy and XPS. Thermal properties of PP thick melamine resin-coated films were analyzed by thermogravimetric analysis. KW - Polymer KW - Plasma KW - Polypropylene KW - Fire retardant KW - Melamine precursors KW - Plasma polymerization KW - Allyl alcohol KW - Flame retardants KW - Curing PY - 2015 DO - https://doi.org/10.1080/01694243.2015.1033878 SN - 0169-4243 SN - 1568-5616 VL - 29 IS - 14 SP - 1522 EP - 1533 PB - VNU Science Press CY - Utrecht AN - OPUS4-33112 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mohamed, Zeinab A1 - Friedrich, Jörg Florian A1 - Krüger, Simone T1 - Cured melamine systems as thick fire-retardant layers deposited by combination of plasma technology and dip-coating N2 - Melamine and melamine resins are widely used as fire-retardants for polymer building materials. Cured melamine systems are used in heat-sensitive items, such as furniture and window frames and sills. In this work, differently cured methylated poly(melamine-co-formaldehyde) (cmPMF) resins were used as fire-retardant coverage for poly(styrene) (PS) and poly(ethylene) (PE) building materials. Such polymer layers should have several tenths of micrometers thickness to produce sufficient fire retardancy. These thick layers were produced by dip-coating. To promote sufficient adhesion of such thick coating to the polyolefin substrates, also in the case of high temperatures occurring at fire exposure, the polymer substrates were firstly coated with a few hundred nanometer thick adhesion-promoting plasma polymer layer. Such thin plasma polymer layers were deposited by low-pressure plasma polymerization of allyl alcohol (ppAAl). It was assumed that the hydroxyl groups of ppAAl interact with the melamine resin; therefore, ppAAl was well suited as adhesion promoter for thick melamine resin coatings. Chemical structure and composition of polymer films were investigated using infrared-attenuated total reflectance and X-ray photoelectron spectroscopy (XPS). Peel strengths of coatings were measured. After peeling, the peeled polymer surfaces were also investigated using optical microscopy and XPS the layers for identification of the locus of peel front propagation. Thermal properties were analyzed using TGA (thermo-gravimetric analyses). Finally, the fire-retardant properties of such thick coated polymers were evaluated by exposure to flames. KW - Plasma polymerization KW - Dip-coating KW - Curing KW - Methylated poly(melamine-co-formaldehyde) KW - Polystyrene KW - Polyethylene KW - Flame retardancy KW - Polymer KW - Plasma KW - Melamine resin KW - Fire retardant PY - 2015 DO - https://doi.org/10.1080/01694243.2014.995911 SN - 0169-4243 SN - 1568-5616 VL - 29 IS - 9 SP - 807 EP - 820 PB - VNU Science Press CY - Utrecht AN - OPUS4-32795 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mohamed, Zeinab A1 - Friedrich, Jörg Florian A1 - Krüger, Simone T1 - Adhesion promotion of thick fire-retardant melamine polymer dip-coatings at polyolefin surfaces by using plasma polymers N2 - Melamine and melamine resins are widely used as fire retardants for polymer materials used in pharmaceutical, plastic, textile, rubber, and construction industry. Melamine-based flame retardants act by blowing off intumescent layers, char formation, and emission of quenching ammonia gas and diluent molecular nitrogen. Special advantages are: low cost, low smoke density and toxicity, low corrosive activity, safe handling, and environmental friendliness. Methylated poly(melamine-co-formaldehyde) (mPMF) was used as thick (≥40 µm) fire-retardant coating for plasma pretreated polymers. A combined low-pressure plasma pretreatment consisting of oxygen plasma exposure followed by deposition of thin poly(allylamine) (ppAAm) and poly(allyl alcohol) (ppAAl) plasma polymers as adhesion promoters have improved the adhesion of thick mPMF coatings strongly. Chemical structure and composition of deposited polymer films were characterized by infrared-attenuated total reflectance and X-ray photoelectron spectroscopy (XPS). After peeling, the peeled layer surfaces were also investigated for identification of the locus of failure and their topography using optical microscopy and XPS. Often the adhesion promotion was so efficient that the peeling of coating was not possible. Thermal properties of plasma polymers and dip-coating films were analyzed by thermogravimetric analysis. Significant improvement of fire-retardant properties of coated polymers was confirmed by flame tests. KW - Adhesion KW - Thick melamine layers KW - Plasma polymerization KW - Dip-coating KW - Methylated poly(melamine-co-formaldehyde) KW - Polystyrene KW - Polyethylene KW - Flame retardancy KW - Fire retardant KW - Melamine resin KW - Polymer KW - Plasma PY - 2014 DO - https://doi.org/10.1080/01694243.2014.943339 SN - 0169-4243 SN - 1568-5616 VL - 28 IS - 21 SP - 2113 EP - 2132 PB - VNU Science Press CY - Utrecht AN - OPUS4-31485 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mix, Renate A1 - Friedrich, Jörg Florian A1 - Neubert, Dietmar A1 - Inagaki, N. T1 - Response of linear, branched or crosslinked polyethylene structures on the attack of oxygen plasma N2 - Linear, branched and crosslinked polyethylenes (PE) were exposed to the low-pressure oxygen plasma for 2–120 s. In the following the samples were washed with solvents to remove low-molecular weight oxidized material and to excavate the subjacent polymer structure for microscopic characterization. X-ray photoelectron spectroscopy (XPS) measurements provided information about changes in elemental composition and chemical structure of PE after plasma exposure and washing. The calculation of the concentration of tertiary C atoms using XPS data was a measure of branches and crosslinking in the polymer before and after exposure to oxygen plasma. Linear PE was most sensitive towards oxygen plasma and showed the highest concentration in tertiary C atoms after plasma exposure. On the other hand branched PE types, which possess originally more tertiary carbon atoms, have lost two-third of them after 2 s oxygen plasma exposure. Branched PE show also topological changes at their surface as detected by atomic force microscopy. Differential scanning calorimetry measurements confirmed strong changes in crystallinity and molecular orientation of linear PE already after 120 s exposure to the oxygen plasma interpreted as amorphization. These effects should be interpreted as result of crosslinking caused by the recombination of dangling bond sites. KW - Linear and branched polyethylene KW - Oxygen plasma KW - Functionalization KW - Crosslinking PY - 2014 UR - http://link.springer.com/article/10.1007%2Fs11090-014-9558-9/fulltext.html DO - https://doi.org/10.1007/s11090-014-9558-9 SN - 0272-4324 VL - 34 IS - 5 SP - 1199 EP - 1218 PB - Plenum Publ. Corp. CY - New York, NY, USA AN - OPUS4-30741 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Mix, Renate A1 - Yin, Huajie A1 - Friedrich, Jörg Florian ED - Gutowski, W. ED - Dodiuk, H. T1 - Aerosol-based DBD - A simple way to provide polymers with functional groups for adhesion promotion N2 - Polypropylene (PP) foils were exposed to the plasma of an atmospheric dielectric barrier discharge (DBD) in presence of different aerosols. Pure liquids such as water, ethanol, and 1/1 mixtures ethanol/water (v/v) or aqueous Solutions of acetic acid, poly(acrylic acid), poly(vinyl alcohol), and ethylene glycolpoly(vinyl alcohol) copolymer were introduced into the DBD. Surface composition, the number of functional groups per 100 C atoms, and water contact angles were correlated with the energy density of DBD plasma exposure. The wettability of the treated surfaces was investigated for different storage times. Peel strength of the thermally deposited aluminum layer to modified polymer surfaces revealed that the aerosol introduction strongly improves the adhesion between aluminum and polypropylene. KW - Aerosol-assisted DBD KW - Functional groups KW - Surface modification PY - 2013 SN - 978-90-04-20173-6 SN - 978-90-04-20174-3 SP - Chapter 8, 155 EP - 170 PB - CRC Press AN - OPUS4-30035 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zeynalov, Eldar A1 - Wagner, M. A1 - Friedrich, Jörg Florian A1 - Magerramova, M. A1 - Salmanova, N. A1 - Hidde, Gundula A1 - Meyer-Plath, A. T1 - The peculiar behavior of functionalized carbon nanotubes in hydrocarbons and polymeric oxidation environments N2 - It has been shown that selected types of substituents are able to vary the oxidative behavior of multi-walled carbon nanotubes. Such substituents investigated were sterically hindered secondary amino groups bonded in grafted piperidine units and covalently bonded bromine groups. Their interference and activity was preliminary determined in the model cumene and then in oil diesel fraction and low density polyethylene oxidation reactions. Results obtained indicate that chemical linking of amine moieties containing –NH groups directly to the carbon nanotubes core significantly increases their intrinsic anti-oxidative capacity while the grafting of Br-groups provokes the opposite functioning of the pristine samples. This inference was proved by thermogravimetric and differential thermal analysis of the polyethylene composites and experiments on profound aerobic oxidation of petroleum naphthenic fraction derived from the commercial Baku oils blend diesel cut. KW - Multi-walled carbon nanotubes KW - Amine derivatives KW - Plasma-chemical technique KW - Brominated carbon nanotubes KW - Rate of model oxidation KW - Anti-oxidative efficiency KW - Catalytic activity KW - Inhibition rate constant KW - Photoelectron spectroscopy KW - Oxidation KW - Polyethylene composites KW - Oil diesel fraction PY - 2016 DO - https://doi.org/10.1080/01694243.2016.1239304 SN - 0169-4243 SN - 1568-5616 VL - 31 IS - 9 SP - 988 EP - 1006 AN - OPUS4-39894 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Mix, Renate A1 - Friedrich, Jörg Florian T1 - Adhesion promotion in metal-polymer composites by introduction of functional groups arranged in a well-defined distance to the polymer surface by spacer incorporation T2 - 10th International Conference on the Science and Technology of Adhesion and Adhesives, Euradh 2008 - Adhesion `08 CY - Oxford, UK DA - 2008-09-03 KW - Adhesion KW - Aluminium KW - Polypropylene KW - Plasma polymers KW - Spacer-bonded functional groups PY - 2008 SP - 447 EP - 451 PB - IOM Communications CY - London AN - OPUS4-18616 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Wettmarshausen, Sascha T1 - A new concept for adhesion promotion in metal-polymer systems by introduction of covalently bonded spacers at the interface N2 - A new concept for molecular interface design in metal-polymer systems is presented. The main features of this concept are the replacement of weak physical interactions by strong covalent bonds, the flexibilization of the interface for compensating different thermal expansions of materials by using long-chain flexible and covalently bonded spacers between the metal and the polymer as well as its design as a moisture-repellent structure for hindering diffusion of water molecules into the interface and hydrolysis of chemical bonds. For this purpose, the main task was to develop plasmachemical and chemical techniques for equipping polymer surfaces with monotype functional groups of adjustable concentration. The establishing of monotype functional groups allows grafting the functional groups by spacer molecules by applying usual wet-chemical reactions. Four processes were favoured for production of monotype functional groups by highly selective reactions: the plasma bromination, the plasma deposition of plasma polymers, the post-plasma chemical reduction of O-functionalities to OH-groups, and the chemical replacement of bromine groups by NH2-groups. The grafting of flexible organic molecules as spacers between the metal layer and polymer improved the peel strength of the metal. To obtain maximal peel strength of aluminium coatings to polypropylene films and occurrence of cohesive failure in the polypropylene substrate, about 27 OH groups per 100 C-atoms or 6 COOH groups per 100 C-atoms were needed. Introducing C6-11-aliphatic spacers 1 OH or COOH group per 100 C-atoms contributed about 60% of the maximal peel strength of the Al-PP system, i.e. 2 or 3 spacer molecules per 100 C-atoms were sufficient for maximal peel strength. KW - Polymer surface functionalization KW - Spacer grafting KW - Metal-polymer adhesion PY - 2008 DO - https://doi.org/10.1163/156856108X309611 SN - 0169-4243 SN - 1568-5616 VL - 22 IS - 10-11 SP - 1123 EP - 1143 PB - VNU Science Press CY - Utrecht AN - OPUS4-17741 LA - eng 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 - JOUR A1 - Joshi, Ranjit A1 - Friedrich, Jörg Florian A1 - Wagner, M.H. T1 - Study of carboxylic functionalization of polypropylene surface using the underwater plasma technique N2 - Non-equilibrium solution plasma treatment of polymer surfaces in water offers the possibility of more dense and selective polymer surface functionalization in comparison to the well-known and frequently used low-pressure oxygen plasma. Functional groups are introduced when the polymer surface contacts the plasma moderated solution especially water solutions. The emission of ions, electrons, energy-rich neutrals and complexes, produced by the ion avalanche are limited by quenching, with the aid of the ambient water phase. The UV-radiation produced in plasma formation also helps to moderate the reaction solution further by producing additional excited, ionized/dissociated molecules. Thus, monotype functional groups equipped polymer surfaces, preferably OH groups, originating from the dissociated water molecules, could be produced more selectively. An interesting feature of the technique is its flexibility to use a wide variety of additives in the water phase. Another way to modify polymer surfaces is the deposition of plasma polymers carrying functional groups as carboxylic groups used in this work. Acetic acid, acrylic acid, maleic and itaconic acid were used as additive monomers. Acetic acid is not a chemically polymerizing monomer but it could polymerize by monomer/molecular fragmentation and recombination to a cross linked layer. The other monomers form preferably water-soluble polymers on a chemical way. Only the fragmented fraction of these monomers could form an insoluble coating by cross linking to substrate. The XPS analysis was used to track the alterations in -O-CO- bond percentage on the PP surface. To identify the -COOH groups on substrate surface unambiguously, which have survived the plasma polymerization process, the derivatization with trifluoroethanol was performed. KW - Polymeroberflächen KW - Funktionelle Gruppen PY - 2009 DO - https://doi.org/10.1140/epjd/e2009-00088-6 SN - 1434-6060 VL - 54 IS - 2 SP - 249 EP - 258 PB - Springer CY - Berlin AN - OPUS4-19607 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Schulze, Rolf-Dieter A1 - Rau, A. T1 - Ultra-thin polymer layer deposition by aerosol-dielectric barrier discharge (DBD) and electrospray ionization (ESI) at atmospheric pressure N2 - Polyolefins are chemically inert and do not adhere well to metals, polymers or inorganics. To overcome this problem, polyolefin surfaces were modified thermally, plasmachemically, or by flame treatment with different oxygen-containing groups, however, unfortunately, such treatments were accompanied by undesired, adhesion lowering polymer degradation. To solve this dilemma, solutions of synthetic polymers and copolymers were prepared, sprayed into the barrier discharge or electrosprayed without discharge and deposited as thin adhesion-promoting layers. The deposited polymer layers from poly(vinylamine), poly(ethylene glycol)-poly(vinyl alcohol) copolymers and poly(acrylic acid) were endowed with monotype functional groups. Using the aerosol - dielectric barrier discharge only a fraction of functional groups survived the deposition process in contrast to the electrospray in which all functional groups were retained. KW - Polymer surface modification KW - Dielectric barrier discharge KW - Polymer aerosols KW - Electrospray deposition KW - Adhesion-promoting layers PY - 2010 DO - https://doi.org/10.1163/016942409X12598231568429 SN - 0169-4243 SN - 1568-5616 VL - 24 IS - 7 SP - 1329 EP - 1350 PB - VNU Science Press CY - Utrecht AN - OPUS4-21374 LA - eng 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 - Friedrich, Jörg Florian T1 - Monosort functionalization of polymer surface as anchoring points for graft syntheses T2 - The Eleventh International Conference on Plasma Surface Engineering, PSE CY - Garmisch-Partenkirchen, Germany DA - 2009-09-15 PY - 2009 AN - OPUS4-18975 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - High selective polymer surface functionalization by using plasmas of Br-containing precursors with low ionization potential T2 - The Eleventh International Conference on Plasma Surface Engineering CY - Garmisch-Partenkirchen, Germany DA - 2009-09-15 PY - 2009 AN - OPUS4-18977 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - New Plasmas for Polymer Surface Functionalization T2 - Vortrag an der Karls-Universität Prag CY - Prague, Czech Republic DA - 2008-01-28 PY - 2008 AN - OPUS4-18978 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Selective Surface Modification of Polypropylene using Underwater Plasma Technique T2 - The Eleventh International Conference on Plasma Surface Engineering CY - Garmisch-Partenkirchen, Germany DA - 2009-09-15 PY - 2009 AN - OPUS4-18979 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Monosort functionalization of polymer surface as anchoring points for graft synthesis T2 - XVI. Erfahrungsaustausch "Oberflächentechnologie mit Plasma- und Ionenstrahlprozessen" CY - Klingenthal, Germany DA - 2009-03-10 PY - 2009 AN - OPUS4-18980 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Chemische Aspekte der Haftung von Metallen auf Polymeren T2 - Workshop Polymerhaftung und Reibung, TU München/Garching CY - Munich, Germany DA - 2008-10-10 PY - 2008 AN - OPUS4-18981 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Polymer Surface Modification by Aerosol Based Corona Treatment of Foils T2 - Eleventh International Conference on Polymer Surface Engineering CY - Garmisch-Partenkirchen, Germany DA - 2008-09-15 PY - 2008 AN - OPUS4-18982 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Unterwasserplasmen zur Funktionalisierung oder Beschichtung von Polymeroberflächen T2 - 16. Neues Dresdner Vakuumtechnisches Kolloquium Beschichtung, Modifizierung und Charakterisierung von Polymeroberflächen (16. NdVak) CY - Dresden, Germany DA - 2008-10-16 PY - 2008 AN - OPUS4-18983 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Plasmabromierung von Polyolefinoberflächen für die chemische Pfropfung T2 - 16. Workshop Plasma- und Ionenstrahltechnologien CY - Klingenthal, Germany DA - 2009-03-10 PY - 2009 AN - OPUS4-19118 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Wettmarshausen, Sascha A1 - Hennecke, Manfred T1 - Neue Molekülarchitekturen an Polyolefinoberflächen T2 - 17. Neues Dresdner Vakuumtechnisches Kolloquium - Beschichtung, Modifizierung und Charakterisierung von Polymeroberflächen CY - Dresden, Deutschland DA - 2009-10-21 KW - Plasma KW - Bromierung KW - Spacer KW - Haftvermittler KW - Metallbedampfung KW - Schälfestigkeit PY - 2009 SN - 978-3-9812550-1-0 SP - 38 EP - 40 AN - OPUS4-20250 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Wettmarshausen, Sascha ED - G. Blasek, T1 - Generelle thermodynamische Probleme bei der Funktionalisierung von Polyolefinoberflächen T2 - 17. Neues Dresdner Vakuumtechnisches Kolloquium - Beschichtung, Modifizierung und Charakterisierung von Polymeroberflächen CY - Dresden, Deutschland DA - 2009-10-21 KW - Plasma KW - Bromierung KW - Spacer KW - Haftvermittler KW - Metallbedampfung KW - Schälfestigkeit KW - Thermodynamik PY - 2009 SN - 978-3-9812550-1-0 SP - 65 EP - 67 AN - OPUS4-20251 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Mix, Renate A1 - Schulze, Rolf-Dieter A1 - Rau, A. A1 - Friedrich, Jörg Florian ED - G. Blasek, T1 - Aerosol-Barriereentladung und Elektrospray zur Polymerschichtabscheidung T2 - 17. Neues Dresdner Vakuumtechnisches Kolloquium - Beschichtung, Modifizierung und Charakterisierung von Polymeroberflächen CY - Dresden, Deutschland DA - 2009-10-21 KW - Corona KW - Barriereentladung KW - Haftvermittler KW - Schälfestigkeit PY - 2009 SN - 978-3-9812550-1-0 SP - 76 EP - 80 AN - OPUS4-20252 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Joshi, Ranjit A1 - Friedrich, Jörg Florian A1 - Wagner, M. T1 - Role of hydrogen peroxide in selective OH group functionalization of polypropylene surfaces using underwater capillary discharge N2 - Plasma chemical methods are well suited for introducing functional groups to the surfaces of chemically inert polymers such as polyolefins. However, a broad variety of functional groups are often formed. Unfortunately, for further chemical processing such as grafting of molecules for advanced applications a highly dense monotype functionalized polyolefin surface is needed. Therefore, the main task was to develop a selective surface functionalization process, which formed preferably only a single type of functional groups at the surface in high concentration. Amongst the novel plasma methods, the underwater plasma process (UWP) is one of most attractive options to solve the problem of monotype functionalization. Such plasma is an efficient source of ions, electrons, UV-radiation, high-frequency shock waves, radicals such as hydroxyl radical, and reactive neutral molecules such as hydrogen peroxide. In contrast to established gas phase glow discharge processes, the water phase limits the particle and radiation energies and thus the energy input into the polymer. By virtue of the liquid water environment, which moderates highly energetic plasma species, extensive oxidation, degradation, cross-linking and radical formation on the polymer are more limited as compared to gas plasma exposure. The variety of plasma produced species in the water phase is also much smaller because of the limited reaction possibilities of the plasma with water. The possibility to admix a broad variety of chemical additives makes underwater plasma even more attractive. Hydrogen peroxide and the catalyst (Fe-ZSM5) should influence and increase the equilibrium concentration of OH radicals in the underwater plasma process. It was found that these radicals played a very important role in OH functionalization of polyolefin surfaces. Hydrogen peroxide was identified to be the most prominent precursor for OH group formation in the UWP. The catalyst would affect the steady state of OH radical formation and its reaction with the substrate surface and thus accelerates the functionalization process. KW - Surface modification KW - Polymer functionalization KW - Underwater plasma KW - Capillary discharge KW - Hydroxyl functionalization KW - Hydrogen peroxide KW - Hydroperoxyl radicals KW - Heterogeneous catalysis KW - Fenton-like processes PY - 2011 DO - https://doi.org/10.1163/016942410X520862 SN - 0169-4243 SN - 1568-5616 VL - 25 SP - 283 EP - 305 PB - VNU Science Press CY - Utrecht AN - OPUS4-22413 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Quasi-Wasserstoffplasma und Nitrilgruppenentstehung T2 - Plasma Germany CY - Dresden, Germany DA - 2010-05-05 PY - 2010 AN - OPUS4-22734 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Adhäsions-Verbesserung der Haftung zwischen Metallen, Carbonanotubes und Polymeren T2 - Vortrag, Chemieverein Erkner CY - Erkner, Germany DA - 2010-03-17 PY - 2010 AN - OPUS4-22735 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Plasma Polymerization Mechanism T2 - Vortrag im Fachausschuß Plasma und Polymere, Plasma Germany CY - Aachen, Germany DA - 2010-11-15 PY - 2010 AN - OPUS4-22736 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Functionalization of polyolefin surfaces and grafting of molecules with complex architecture T2 - ASPC Leoben CY - Leoben, Austria DA - 2010-09-08 PY - 2010 AN - OPUS4-22737 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - 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 - 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 - JOUR A1 - Zeynalov, Eldar A1 - Friedrich, Jörg Florian T1 - Antioxidative Activity of Carbon Nanotube and Nanofiber N2 - Carbon nanotubes (CNTs) and carbon nanofibers (CNFs) have electron affinities similar to those of fullerenes C60 and C70 and they are therefore capable of acting as radical scavengers in free radical chain reactions, including polymerisation and the thermo-oxidative degradation of polymers. It is assumed that the CNTs and CNFs used as integral part of polymer composites are able to exhibit an antioxidant effect in these materials because of their radical accepting capacity. To examine this presumption the antioxidative activity of original and purified commercial multiwall carbon nanotube MWCNT and carbon nanofibre of platelet structure CNF-PL has been studied by means of a model oxidation reaction of cumene initiated (2,2'-azobisisobutyronitrile, AIBN) in liquid phase. This model reaction was designed to simulate the thermo-oxidative processes in carbon-chain polymers and allows comparison and transfer of obtained results to a polymer system. Kinetic measurements of oxidation rates showed that the effect of inhibition for the model oxidative reaction in the presence of the original and purified MWCNT and CNF-PL strongly depends on the presence of metals (Co, Fe) in the nanoparticles. Rates of oxidation Wo2 (CNT;CNF) observed for the unrefined samples are result of the two competing rates - rate of inhibition Winh.(CNT; CNF) caused by structures of the CNT or CNF and the rates of initiation Wi(M) due to the following interaction: ROOH + M (Co;Fe) i.e, Wo2 ~ W inh (CNT;CNF) + Wi(M). The effective rate constants for the addition of cumyl radicals (R.) to MWCNT and CNF-PL have been determined. These constants reduced to the same concentration (0.5wt.%) and temperature (60°C) units have magnitudes: k1(MWCNT) [MWCNT] = (2.8 ± 0.3) x104 s-1and k1(CNF) [CNF] = (6.0 ± 1.0) x103 s-1. Thus, the effective rate constant, reflecting the antioxidative activity for the CNT, is five times higher than that for the CNF, is about equal to the rate constant for HAS Chimassorb 2020: k1(Chim.2020)[Chim. 2020] = (2.2 ± 0.3) x104 s-1, is ten times less than that for the HAS Chimassorb 119FL: k1(Chim.119FL)[Chim. 119FL] = (2.8 ± 0.3) x105 s-1 and is about forty times less than that for the case of fullerene C60: k1(C60)[C60](353K) = (1.2 ± 0.2) x106 s-1. The kinetic data obtained specify the level of original antioxidative activity of MWCNTs and CNFs and scope of their rational use in polymer composites. It is believed that the results will be helpful for designing optimal profile of polymer composites filled by the CNT/CNFs. KW - Model oxidation KW - Carbon nanotubes KW - Carbon nanofibres KW - Kinetics KW - Oxidation rate KW - Inhibiting activity KW - Rate constant PY - 2008 DO - https://doi.org/10.2174/1874088X00802010028 SN - 1874-088X VL - 2 IS - 1 SP - 28 EP - 34 PB - Bentham Open AN - OPUS4-17839 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Joshi, Ranjit A1 - Friedrich, Jörg Florian T1 - Unterwasserplasma zur Funktionalisierung oder Beschichtung von Polymeroberflächen T2 - 16. Neues Dresdner Vakuumtechnisches Kolloquium - Beschichtung, Modifizierung und Charakterisierung von Polymeroberflächen CY - Dresden, Deutschland DA - 2008-10-16 KW - Polymer-Oberflächenfunktionalisierung PY - 2008 SN - 978-3-9812550-0-3 SP - 44 EP - 52 AN - OPUS4-18315 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 - JOUR A1 - Zeynalov, Eldar A1 - Aliyeva, A. Z. A1 - Friedrich, Jörg Florian T1 - Factors affecting the intrinsic anti-oxidative activity of carbon-nanofibers - Metallic impurities N2 - Nanotubes und Nanofasern (CNT, CNF) besitzen inhärente antioxidative Eigenschaften. Diese Fähigkeit könnte sehr nützlich für die Langzeitstabilität entsprechender Polymercomposite sein. Sie haben Elektronenaffinitäten ähnlich der von Fullerenen und sind deshalb in der Lage, Radikalfallen darzustellen und damit radikalische Kettenreaktionen zu unterbinden. Hier wurde die anti-oxidative Aktivität kommerzieller Nanofasern von Fischgrätenstruktur untersucht. Zunächst wurde der quantitative Einfluss von Ni-Verunreinigungen erfasst. Die eigentliche anti-oxidative Wirkung wurde mit einer aeroben Modelloxidation von Cumol verifiziert und deren kinetischen Parameter für kommerzielle und besonders gereinigte CNF-HBs bestimmt. CNF-HB inhibiert die Modellreaktion durch Einfangen der Peroxiradikale. Die Oxidation vollzieht sich nach einer ausgeprägten Induktionsphase in semi-logarithmischer Abhängigkeit für die speziell gereinigten Spezies. Es konnten erstmals die effektive Konzentration an inhibierenden Zentren und die Inhibierungs-Geschwindigkeitskonstante für CNF-HB bestimmt werden. Die Inhibierungs-Geschwindigkeitskonstante beträgt k7 = (6 ± 1.0) × 103lmol-1 s-1 und liegt damit in der für Anti-Oxidanzien erwarteten Größenordnung. KW - Nanotubes KW - Radical scavenger KW - Anti-oxidative behaviour PY - 2009 SN - 0025-5300 VL - 51 IS - 4 SP - 210 EP - 214 PB - Hanser CY - München AN - OPUS4-19253 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 - JOUR A1 - Wohlrab, Sebastian A1 - Schönhals, Andreas A1 - Goering, Harald A1 - Friedrich, Jörg Florian T1 - Integration of sol-gel derived inorganic nanonetworks into polymers N2 - Nanoparticulate networks as fillers for polymer based nanocomposites offer an optimized, surfactant free distribution of the inorganic component. Additionally, their non-aggregated but interconnected nanoparticulate subunits can lead to new properties owing to special inherent solid state properties and/or spacial restrictions to the polymeric parts. In particular, polymer nanocomposites based on poly(methyl methacrylate) (PMMA) or poly(hydroxyethyl methacrylate) (PHEMA), filled with different nanoparticulate networks of AlOOH were synthesized using two advanced synthesis techniques. An ex situ method, in which a preformed AlOOH-gel was solvent exchanged by methyl methacrylate (MMA) and an in situ method, in which the AlOOH scaffold was prepared within hydroxyethyl methacrylate (HEMA), have been used to produce the materials described here through polymerization. On the MMA based composites the particles were removed by etching, yielding porous polymers. Promising for a broad variety of crystallisable networks within polymers, the phase transition of amorphous AlOOH within PMMA towards crystalline boehmite was performed using a hydrothermal method. The materials were characterized using transmission electron microscopy, X-ray diffraction, gel permeation chromatography, differential scanning calorimetry, IR-spectroscopy, UV/Vis spectroscopy and hardness measurements. Special material properties were investigated using thermogravimetry, thermomechanical analysis and dynamic mechanical analysis. Furthermore, interactions between PMMA segments and the AlOOH network were detailed studied using dielectric spectroscopy. PY - 2010 DO - https://doi.org/10.1039/c0py00105h SN - 1759-9954 SN - 1759-9962 VL - 1 IS - 8 SP - 1226 EP - 1236 AN - OPUS4-21996 LA - eng 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 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Kühn, Gerhard T1 - Functional groups bearing plasma homo and copolymer layers as adhesion promoters in metal-polymer composites N2 - Functional groups bearing monomers were pulsed plasma polymerised with a degree of retained functional groups of 55–91%. The following functional groups could be produced at a maximum of: 30 OH, 18 NH2, and 24 COOH per 100 C atoms. A plasma-initiated radical copolymerisation could also be realised using the functional group bearing monomers as a source of functionalities, olefins as ‘chain-extenders’ and dienes as ‘chemical cross-linkers’. The peel strengths of Al layers on such plasma polymers were correlated to the type and density of functional groups. KW - Functional groups KW - Adhesion promoters KW - Metal-polymer composites PY - 2003 DO - https://doi.org/10.1016/S0257-8972(03)00350-5 SN - 0257-8972 VL - 174-175 SP - 811 EP - 815 PB - Elsevier Science CY - Lausanne AN - OPUS4-2703 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Mix, Renate A1 - Fritz, Andreas A1 - Schönhals, Andreas T1 - Polymer surface modification with monofunctional groups of variable types and densities N2 - The retention of chemical structure and functional groups during pulsed plasma polymerization was used for producing adhesion-promoting plasma polymer layers with high concentrations of exclusively one kind of functional groups, such as OH, NH2, or COOH. The maximum content of functional groups was 31 OH using allyl alcohol, 18 NH2 using allylamine, or 24 COOH per 100 C atoms using acrylic acid. To vary the density of functional groups, chemical co-polymerization with ethylene as 'chain-extending' co-monomer, or butadiene as 'chemical crosslinker' was initiated in the pulsed plasma. The composition of these co-polymers was investigated by XPS and IR spectroscopy. The concentrations of functional groups were measured by derivatizing with fluorine-containing reagents and using XPS. A set of plasma parameters was found to be a good compromise between a high number of functional groups and complete insolubility in water, ethanol or THF,which is needed for further chemical processing. Here, these monotype-functionalized surfaces were used in metal-polymer systems as adhesion-promoting interlayers to examine the influence of type and density of functional groups on adhesion. As expected, COOH- and OH-group-terminated interlayers showed maximum peel strengths to evaporated aluminium layers. The adhesion increased linearly with the number of OH groups to a maximum at about 27 OH per 100 C atoms. Higher concentrations of OH groups did not increase the peel strength further. KW - Co-polymers KW - Adhesion-promoting interlayers KW - Metal-polymer systems PY - 2003 DO - https://doi.org/10.1163/156856103322396695 SN - 0169-4243 SN - 1568-5616 VL - 17 IS - 12 SP - 1591 EP - 1617 PB - VNU Science Press CY - Utrecht AN - OPUS4-2704 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Koprinarov, Ivaylo A1 - Ghode, Archana A1 - Geng, Sh. A1 - Kühn, Gerhard T1 - Plasma-based introduction of monosort functional groups of different type and density onto polymer surfaces. Part 1: Behaviour of polymers exposed to oxygen plasma N2 - Several approaches were investigated to produce monosort functionalized polymer surfaces with a high density and homogeneity of functional groups: (i) Plasma oxidation followed by wet-chemical reduction, (ii) formation of radicals and grafting on of functional group carrying molecules, (iii) plasma bromination followed by (iv) Williamson or Gabriel-like synthesis of spacer molecules, and (v) a pulsed plasma polymerization of functional groups bearing monomers or (vi) their copolymerisation with other comonomers. The formation of hydroxyl (OH), primary amino (NH2), and carboxyl (COOH) groups was studied in detail. The oxygen plasma treatment (i) in a low-pressure non-isothermal glow discharge results in the formation of a wide variety of O functional groups, polymer degradation and crosslinking. Low power densities and short exposure times (0.1 to 2 s) are required to functionalize a surface while preserving the original polymer structure. Carbonate, ester, and aromatic groups are rapidly degraded by an oxygen plasma treatment leading to scissions of polymer backbones and loss in molecular weight. Also the formation of macrocycles and C=C bonds was observed in a region of around 4 nm in depth. The investigated polymers could be classified by their degradation behaviour on exposure to the oxygen plasma.___TAGSTART___BR___TAGEND___ In order to maximize the process selectivity for OH groups, the variety of oxygen functionalities formed by the oxygen plasma was wet-chemically reduced by diborane, vitridetrade (Na complex), and LiAlH4. Typical yields were 9 to 14 OH groups per 100 carbon atoms.___TAGSTART___BR___TAGEND___ Plasma bromination (iii) (40 Br per 100 C atoms) of polymers, followed by grafting of spacer molecules (iv), has been proved to be a highly selective reaction.___TAGSTART___BR___TAGEND___ Another way to produce high densities of monosort functionalities was the pulsed plasma polymerization of functional group bearing monomers such as allylamine, allylalcohol or acrylic acid (v). The retention of chemical structure and functional groups during plasma polymerization was achieved by using low power densities and the pulsed plasma technique. The maximum yields were 30 OH, 18 NH2, and 24 COOH groups per 100 C atoms. To vary the density of functional groups a chemical copolymerization with ''chain-extending'' comonomers such as butadiene and ethylene was initiated in the pulsed plasma (vi). Additionally, the often-observed post-plasma oxidations of such layers initiated by reaction of trapped radicals with oxygen from the air were successfully suppressed by using NO gas as radical quencher. PY - 2003 DO - https://doi.org/10.1163/156855403765826865 VL - 10 IS - 2-3 SP - 139 EP - 171 PB - North-Holland CY - New York, NY AN - OPUS4-2705 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Kühn, Gerhard A1 - Retzko, Iris A1 - Schönhals, Andreas A1 - Unger, Wolfgang T1 - Plasma-based introduction of monosort functional groups of different type and density onto polymer surfaces. Part 2: Pulsed plasma polymerization N2 - This new functionalization method consists of the deposition of very thin plasma polymer layers (20 to 100 nm) of functional group bearing monomers in pulsed plasma. With allylalcohol, a maximum of 30 OH groups per 100 C atoms was measured with a selectivity of about 90% and a significant stability at long-time exposure to air. Allylamine was used to produce primary amino groups, with a maximum of 18 NH2 groups per 100 C atoms. Side reactions were observed during the storage in air, such as oxidation of the amino groups. Carboxylic groups could be produced using acrylic acid with a maximum concentration of 24 COOH groups per 100 C atoms. The most prominent side reaction was the decarbonylation/ decarboxylation of the acid group during plasma deposition.___TAGSTART___BR___TAGEND___ The variation of the density of functional groups using the pulsed-plasma polymerization of functional-group-bearing monomers was possible by the chemically-initiated radical copolymerization with either a chain-extending monomer, such as ethylene, or a cross linker, such as butadiene, in plasma. The density of functional groups could be adjusted continuously (0 to 30 OH, 0 to 18 NH2 and 0 to 24 COOH groups per 100 C atoms).___TAGSTART___BR___TAGEND___ The successful application of these densely functionalized polymer surfaces for producing biocompatible surfaces and for use in metal–polymer composites is proposed. KW - Pulsed plasma polymerization KW - Plasma-initiated copolymerization KW - Charcterization of homo- and copolymers PY - 2003 DO - https://doi.org/10.1163/156855403765826874 VL - 10 IS - 2-3 SP - 173 EP - 223 PB - North-Holland CY - New York, NY AN - OPUS4-2706 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Schulz, Ulrich A1 - Jansen, Kirsten A1 - Bertus, Angela A1 - Fischer, S. A1 - Möller, B. T1 - Characterization of fluorinated polyethylene surfaces N2 - Polyethylene foils, used as greenhouse foils stabilized with various types of sterically hindered amine light stabilizers (HALS), showed an extraordinary prolonged lifetime on exposure to natural or artificial weathering if a gas-phase fluorination under low-pressure conditions was applied. The fluorination was performed using F2/N2 mixtures and provided ca. 50 F/100 C (fluorination degree ap25%). The lifetimes of fluorinated PE foils on exposure to artificial or natural weathering were increased at least by a factor of 2-4 as measured in terms of tensile strength and elongation at break. KW - Gas phase fluorination of PE KW - Fluorination kinetics KW - Weathering PY - 2003 DO - https://doi.org/10.1163/156856103322113832 SN - 0169-4243 SN - 1568-5616 VL - 17 IS - 8 SP - 1127 EP - 1143 PB - VNU Science Press CY - Utrecht AN - OPUS4-2707 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulze, Rolf-Dieter A1 - Mix, Renate A1 - Kühn, Gerhard A1 - Friedrich, Jörg Florian ED - d'Agostino, R. T1 - Pulsed plasma initiated homo and copolymerisation - deposition rates and plasma diagnostics in dependence on the pulse length and frequency 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 - OPUS4-2708 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 - Friedrich, Jörg Florian A1 - Schönhals, Andreas A1 - Fritz, Andreas A1 - Mix, Renate A1 - Kühn, Gerhard ED - d'Agostino, R. T1 - Pulsed plasma initiated homo and copolymerisation - characterization of thin plasma polymer layers by dielectric relaxation spectroscopy 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 - OPUS4-2711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Mix, Renate ED - d'Agostino, R. T1 - Polymer surface modification with monofunctional groups of different type and density 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 - OPUS4-2712 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Mix, Renate A1 - Unger, Wolfgang T1 - Formation of Plasma Polymer Layers with Functional Groups of Different Type and Density at Polymer Surfaces and their Interaction with Al Atoms N2 - Monotype functionalizations with different types of functional groups (OH, NH2, COOH) on polypropylene and poly(tetrafluoroethylene) surfaces were synthesized using pulsed plasma-initiated homo- or copolymerization of functional group-carrying monomers. The maximum concentrations of functional groups were 31 OH, 18 NH2 or 24 COOH groups per 100 C atoms using allyl alcohol, allylamine or acrylic acid respectively as the monomer. The measured peel strengths of aluminium deposits increased linearly with the concentration of functional groups. Near the maximum concentration of OH (>27 OH/100 C atoms) or at moderate concentrations of COOH groups (>10 COOH/100 C atoms), constant (maximum) peel strengths were measured due to the mechanical collapse of one component in the composite (cohesive failure). Interface failures in Al-PP composites were found with COOH, NH2 and OH groups and cohesive failures were seen when higher concentrations of COOH groups were applied (>10 COOH/100 C atoms). PY - 2004 DO - https://doi.org/10.1002/ppap.200400008 SN - 1612-8850 SN - 1612-8869 VL - 1 IS - 1 SP - 28 EP - 50 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-4707 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Oran, Umut A1 - Swaraj, Sufal A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang T1 - Surface analysis of plasma-deposited polymer films, 1: Time of Flight Static Secondary Ion Mass Spectrometry (ToF-SSIMS) of plasma polystyrene before and after exposure to ambient air N2 - Pulsed plasma-deposited polystyrene films were studied by time-of-flight static secondary ion mass spectrometry (ToF-SSIMS) before and after exposure to ambient air. The influence of the external plasma parameters on the secondary ion mass spectra of plasma-deposited polystyrene films was investigated. From these data, information on the chemical character of the plasma polystyrene films was derived. In the range of deposition conditions applied in this study, the fragmentation of styrene is a minor process. The main process is probably the radical chain propagation to polymers. All the polystyrene plasma polymers, relying on ToF-SIMS, seem to be rather similar to a reference polystyrene oligomer sample. When the plasma polymers are exposed to air, extensive oxygen incorporation occurs. Oxygen uptake was found to alter the emission probabilities of secondary ions. A relation between the regularity of the plasma polymers and the amount of oxygen incorporation was found. The result was that the chemical regularity of the plasma polystyrene decreases when the effective power in the plasma is increased. PY - 2004 DO - https://doi.org/10.1002/ppap.200400002 SN - 1612-8850 SN - 1612-8869 VL - 1 SP - 123 EP - 133 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-4697 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Quantitative Measuring of C Radical Sites at Polymer Surfaces using the Derivatization Technique and XPS T2 - ECASIA `03 CY - Berlin, Germany DA - 2003-10-06 PY - 2003 AN - OPUS4-4676 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Kühn, Gerhard T1 - Contribution of chemical interactions to the adhesion between aluminium and functional groups of different (mono-) type and density at polymer surfaces T2 - 7th European Adhesion Conference (EURADH 2004) CY - Freiburg im Breisgau, Germany DA - 2004-09-07 PY - 2004 VL - 1 SP - 138 EP - 143 PB - DECHEMA CY - Frankfurt am Main AN - OPUS4-4680 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian T1 - Ein neues Polymerisationsverfahren T2 - Berliner Polymertage 2000 (Humboldt Universität zu Berlin) CY - Berlin, Germany DA - 2000-10-11 PY - 2000 AN - OPUS4-6119 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Swaraj, Sufal A1 - Oran, Umut A1 - Lippitz, Andreas A1 - Schulze, Rolf-Dieter A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang T1 - Surface Analysis of Plasma-Deposited Polymer Films, 2: Analysis of Post-Plasma Air Reacted Plasma Polymerized Styrene by X-Ray Photoelectron Spectroscopy and X-Ray Absorption Spectroscopy N2 - Chemical properties of plasma-polymerized styrene films can be effectively controlled by the appropriate choice of external plasma parameters, such as duty cycle, power and monomer pressure. Chemical properties here are the regularity of the primary structure, the amount of long living radicals and branching or cross-linking or both in plasma polymerized styrene films, which can be indirectly monitored by X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. Principally, XPS and NEXAFS spectra of plasma-polymerized styrene show all the spectroscopic fingerprints characteristic of atactic polystyrene indicating an inherent similarity of the respective primary chemical structures. There is an increase in irregularity and radical concentration for the plasma deposited films with increasing duty cycle or power. With an increase in monomer pressure, a decreased level of monomer fragmentation and, consequently, an increase in regularity must be concluded from the experimental data. The applied power regulates the fragmentation of the monomers as monitored by spectroscopic signals correlated to the aromatic rings. A trend in the extent of the post-plasma oxygen incorporation according to the variation of the various external plasma parameters was deduced, which agrees with earlier ToF-SIMS findings KW - Chemical characterization KW - ESCA/XPS KW - NEXAFS KW - Plasma polymerization KW - Polystyrene PY - 2004 DO - https://doi.org/10.1002/ppap.200400022 SN - 1612-8850 SN - 1612-8869 VL - 1 SP - 134 EP - 140 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-6935 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Oran, Umut A1 - Swaraj, Sufal A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang T1 - Surface Analysis of Plasma-Deposited Polymer Films, 3: In situ Characterization of Plasma-Deposited Ethylene Films by ToF-SSIMS N2 - Pulsed-plasma-deposited ethylene films were studied by time-of-flight static secondary ion mass spectrometry (ToF-SSIMS) before and after exposure to ambient air. The influence of the external plasma parameters on the secondary ion mass spectra of plasma-deposited ethylene films was investigated. From these data, information on the chemical character of the plasma-deposited ethylene films was derived. The investigation of the effect of external plasma parameters on the chemical character of the plasma-deposited ethylene films revealed that there were some drastic changes in the secondary ion mass spectra of the films. It was found that fragmentation and re-arrangement of the monomer molecules in the plasma, which affects the chemical character of the deposited films, vary according to the external plasma parameters. When the plasma polymers are exposed to air, extensive oxygen incorporation occurs. The oxygen uptake is high at the beginning and then it levels of. Some indications for the formation and decay of peroxy radicals (COO) and, subsequently, hydroperoxides (COOH) are found. It was observed that the oxygen uptake of the plasma deposited ethylene films increase when the plasma conditions become harder. KW - Ageing KW - Plasma polymerization KW - Polyethylene (PE) KW - ToF-SIMS PY - 2004 DO - https://doi.org/10.1002/ppap.200400025 SN - 1612-8850 SN - 1612-8869 VL - 1 SP - 141 EP - 152 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-6936 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Retzko, Iris A1 - Friedrich, Jörg Florian A1 - Lippitz, Andreas A1 - Unger, Wolfgang T1 - Chemical analysis of plasma-polymerized films: The application of X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (NEXAFS) and fourier transform infrared spectroscopy (FTIR) N2 - Selected FTIR, XPS and NEXAFS spectroscopy results obtained with films deposited with different plasma polymerization processes and different monomers (styrene, acetylene, ethylene and butadiene) are presented. In detail FTIR spectra, XPS surveys, XPS valence bands and core level signals including shake-up features as well as carbon K-edge absorption spectra are qualitatively and, in some cases, semi-quantitatively considered. Information on the film formation, the chemistry of the films and the film stability against air exposure are derived from spectroscopic features. With styrene chemically rather well defined plasma polymer layers can be formed with rather high deposition rates applying a pulse plasma process. Using ethylene, acetylene or butadiene as a monomer in the plasma deposition process the deposition rates are smaller. Using these monomers plasma polymer films can be obtained with a primary chemical structure which is similar to each other but more or less different from those of the respective conventional polymers. The main difference between these samples is their individual concentration of unsaturated carbon species. Finally, a technologically relevant example, i.e. a plasma deposited polymer barrier layer deposited on the inner wall of a poly(ethylene) vessel is briefly considered. KW - Plasma polymer KW - Styrene KW - Ethylene KW - Acethylene KW - Butadiene KW - XPS KW - NEXAFS KW - FTIR KW - Chemical characterization KW - Deposition process KW - Stability PY - 2001 DO - https://doi.org/10.1016/S0368-2048(01)00330-9 SN - 0368-2048 SN - 1873-2526 VL - 121 IS - 2 SP - 111 EP - 129 PB - Elsevier CY - Amsterdam AN - OPUS4-6938 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mach, Reinhard A1 - Letzig, U. A1 - Goering, Harald A1 - Oleszak, Franz A1 - Friedrich, Jörg Florian A1 - Richter, K. T1 - Effects of Heat Treatment on the Structure of Thermal Plasma Synthesized SiCN Composite Nanopowders N2 - SiCN composite nanopowders with different chemical composition and characteristics were synthesized by the RF induction plasma at atmospheric pressure. Frequently the as-produced powders exhibit a high degree of chemical disorder or structural defects. Because the composition and the microstructure of starting powders have a great influence on the properties of composite ceramics, the changes of chemical composition, crystallization, and morphology of the as-produced powders during heat treatment up to 1500 °C were investigated in detail. PY - 2003 UR - http://www.ipme.ru/e-journals/RAMS/no_1503/tai/tai.html SN - 1606-5131 VL - 5 IS - 1 SP - 85 EP - 90 PB - Advanced Study Center CY - St. Petersburg AN - OPUS4-6968 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Unger, Wolfgang A1 - Mix, Renate ED - Radusch, H.-J. ED - Fiedler, L. T1 - Plasma-initiated homo and copolymerisation for modifying polymer surfaces with funtional groups of different type and density T2 - Internationale Fachtagung Polymerwerkstoffe ; P-2002 CY - Halle (Saale), Germany DA - 2002-09-25 PY - 2002 SN - 3-86010-656-2 SP - 534 EP - 539 PB - Martin-Luther-Univ. Halle-Wittenberg CY - Halle (Saale) AN - OPUS4-6969 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Mix, Renate A1 - Kühn, Gerhard A1 - Unger, Wolfgang T1 - Functional groups bearing plasma homo and copolymer layers as adhesion promoters in metal-polymer composites T2 - 10. Neues Dresdner Vakuumtechnisches Kolloquium (NDVaK) CY - Dresden, Germany DA - 2002-10-17 PY - 2002 SP - 6 EP - 15 PB - DTVa CY - Dresden AN - OPUS4-6970 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kühn, Gerhard A1 - Retzko, Iris A1 - Lippitz, Andreas A1 - Unger, Wolfgang A1 - Friedrich, Jörg Florian T1 - Homofunctionalized polymer surfaces formed by selective plasma processes N2 - Several possibilities exist to produce a modified polymer surface with a high density of only one sort of functional group such as: (i) the plasma grafting of unfragmented monomer molecules and their polymerization forms OH, NH2, COOH groups, etc. in concentrations of approximately 25 groups per 100 C atoms; (ii) selective plasma bromination provides 10–25 CBr groups; (iii) the plasma oxidation of polymer surfaces in an O2 plasma followed by the chemical reduction of all O-containing groups to OH groups by diborane, vitride™ (Na complex) or LiAlH4 yields 9–14 OH groups per 100 carbon atoms; and (iv) the grafting of spacers with different endgroups onto OH or CBr groups produces 7–10 spacer molecules/100 C. This work was focused on the formation of thin plasma deposited polymer layers with a maximum of (homo)functional groups and with a minimum of chemical irregularities using the pulsed plasma technique. The monomers were allylalcohol, allylamine, acrylonitrile and acrylic acid. The further intent was to study the interactions of functional groups (OH, COOH, NH2) and deposited metals (Cr, Al, Ti). It was expected that more basic (NH2), weakly basic or neutral (OH) or more acidic (COOH) groups would show different interactions and chemical reactions with metal atoms. KW - Pulsed plasma polymerization KW - Functional groups KW - Long-term stability KW - Polymer-metal composites PY - 2001 DO - https://doi.org/10.1016/S0257-8972(01)01056-8 SN - 0257-8972 VL - 142-144 SP - 494 EP - 500 PB - Elsevier Science CY - Lausanne AN - OPUS4-6971 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Retzko, Iris A1 - Kühn, Gerhard A1 - Unger, Wolfgang A1 - Lippitz, Andreas T1 - Plasma polymers with chemically defined structures in contact with metals N2 - The retention of chemical structure and functional groups during plasma polymerization was investigated. Usually plasma polymer layers, prepared by a continuous wave radio-frequency plasma, are often chemically irregular in their structure and composition. To minimize these irregularities low wattages and the pulsed plasma technique were applied to avoid fragmentations. The first goal was to produce plasma polymers comprising double or triple bonds as precursors for electrically conducting polymers. Acetylene, ethylene, butadiene and polystyrene were used as monomers and deposited as thin polymer films by pulsed plasmas of low wattages. Styrene polymerization was strongly enhanced in the dark phase (plasma off) of a pulsed r.f. plasma caused by the reactivity of the vinyl-type double bond. This could be confirmed by a verification of a rather high chemical regularity of the film sample. The oxygen content of this film measured by X-ray photoelectron spectrometry (XPS) was in situ 0% and after 24 h exposure to air lower than 1%. Additionally, post-plasma oxidations of trapped radicals with air could be suppressed using NO gas as radical quencher. Such quenched plasma polymer layers were completely stable against oxidation for a number of weeks. During the low-wattage pulse plasma polymerization metal atoms were simultaneously or layer by layer evaporated into the growing layer and in situ measured by XPS. These metal atoms are acting as dopants. Here, Li, K, Mg and Cr were used at different concentrations providing electrical conductivity and magnetic properties for the film. KW - Pulsed plasma KW - Plasma polymerization KW - Doping with metal atoms KW - Encapsulation of nanoparticles PY - 2001 DO - https://doi.org/10.1016/S0257-8972(01)01051-9 SN - 0257-8972 VL - 142-144 SP - 460 EP - 467 PB - Elsevier Science CY - Lausanne AN - OPUS4-6972 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Möller, B. A1 - Kühn, Gerhard A1 - Unger, Wolfgang A1 - Krüger, P. T1 - Improvement of adhesion properties of polymers by producing oxyfluorinated surfaces PY - 2001 SN - 0016-4232 VL - 92 IS - 5 SP - 1334 EP - 1444 PB - Leuze CY - Saulgau, Württ. AN - OPUS4-6973 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Retzko, Iris A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Lippitz, Andreas A1 - Unger, Wolfgang T1 - Eine neue Generation von alterungsbeständigen Plasmapolymeren mit definierter chemischer Struktur T2 - 8. Neues Dresdner Vakuumtechnisches Kolloquium (NDVaK) CY - Dresden, Deutschland DA - 2000-10-19 PY - 2000 VL - 8 SP - 110 EP - 114 CY - Dresden AN - OPUS4-6974 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, P. A1 - Knes, R. A1 - Friedrich, Jörg Florian T1 - Surface cleaning by plasma-enhanced desorption of contaminants PY - 1999 SN - 0257-8972 VL - 112 SP - 240 EP - 244 PB - Elsevier Science CY - Lausanne AN - OPUS4-6984 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Koprinarov, Ivaylo A1 - Friedrich, Jörg Florian A1 - Wöll, Ch. T1 - K-Edge Soft X-ray Absorption (NEXAFS) Spectroscopy In Surface Chemical Analysis of Polymers T2 - International Discussion Meeting Advanced Methods of Polymer Characterization: New Developments and Applications in Industry CY - Mainz, Germany DA - 1999-03-15 PY - 1999 SP - P3.53 CY - Mainz AN - OPUS4-6925 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Grytsenko, K. A1 - Grynko, D. A1 - Lozovski, V. A1 - Friedrich, Jörg Florian A1 - Schulze, Rolf-Dieter A1 - Jurga, J. A1 - Convertino, A. A1 - Kotko, A. ED - Jurga, J. T1 - Properties of Au nano-clusters in PTFE film prepared by co-evaporation in a vacuum PY - 2004 SN - 83-7143-232-1 SP - 79 EP - 84 PB - Wydawn. Politechniki Pozna´nskiej CY - Poznan AN - OPUS4-6961 LA - eng 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 - JOUR A1 - Geng, Sh. A1 - Friedrich, Jörg Florian A1 - Gähde, J. A1 - Guo, L. T1 - Surface-Enhanced Infrared Absorption (SEIRA) and Its Use in analysis of Plasma-Modified Surface KW - Plasma KW - IR KW - Surface-enhanced infrared absorption (SEIRA) KW - Surface modification PY - 1999 SN - 0021-8995 SN - 1097-4628 VL - 71 SP - 1231 EP - 1237 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-6985 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Friedrich, Jörg Florian A1 - Koprinarov, Ivaylo A1 - Weiss, K. A1 - Wöll, Ch. ED - Mittal, K. T1 - The Application of Near Edge X-ray Absorption Fine Structures (NEXAFS) Spectroscopy and X-ray Photoelectron Spectroscopy (XPS) in Surface Analysis of Chromium-evaporated Polymers and Organic Films PY - 1998 SN - 90-6764-290-8 SP - 147 EP - 168 PB - VSP CY - Utrecht AN - OPUS4-6986 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Koprinarov, Ivaylo A1 - Lippitz, Andreas A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang A1 - Wöll, Ch. T1 - Oxygen plama induced degradation of the surface of poly(styrene), poly(bisphenol-A-carbonate) and poly(ethylene terephthalate) as observed by soft X-ray absorption spectroscopy (NEXAFS) KW - Oxygen DC plasma treatment KW - Plasma degradation KW - X-ray absorption spectroscopy (NEXAFS) PY - 1998 SN - 0032-3861 SN - 1873-2291 VL - 39 IS - 14 SP - 3001 EP - 3009 PB - Springer CY - Berlin AN - OPUS4-6990 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Koprinarov, Ivaylo A1 - Giebler, Rainer A1 - Lippitz, Andreas A1 - Unger, Wolfgang T1 - Reactions and Intermediates at the Metal-Polymer Interface - Detected by XPS and NEXAFS Spectroscopy T2 - 4th European Conference on Adhesion (EURADH '98) ; 1st World Congress on Adhesion and Related Phenomena (WCARP) CY - Garmisch-Partenkirchen, Germany DA - 1998-09-06 PY - 1998 SN - 0021-8464 VL - 75 IS - 1 SP - 1.60 EP - 1.62 PB - Gordon & Breach CY - New York, NY AN - OPUS4-6991 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Krüger, P. A1 - Friedrich, Jörg Florian ED - Mennig, G. T1 - Modifizierung von Polymeren im Niederdruckplasma T2 - 15. Fachtagung über Verarbeitung und Anwendung von Polymeren CY - Chemnitz, Deutschland DA - 1997-11-13 PY - 1997 SN - 3-00-001942-1 IS - B27 SP - 1 EP - 8 PB - Techn. Univ. CY - Chemnitz AN - OPUS4-6992 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, P. A1 - Wigant, L. A1 - Friedrich, Jörg Florian ED - Nowack, H. T1 - Permeabilitätsverminderung von Polyolefinfilmen durch Plasmapolymerbeschichtungen T2 - 5. Internationale Fachtagung - ND-Plasma-Technologie CY - Duisburg, Deutschland DA - 1997-09-22 PY - 1997 VL - 5 SP - 1(?) EP - 16(?) PB - Print-Service CY - Mülheim AN - OPUS4-6996 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Koprinarov, Ivaylo A1 - Lippitz, Andreas A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang A1 - Wöll, Ch. T1 - Surface analysis of DC oxygen plasma treated or chromium evaporated poly(ethylene terephthalate) foils by soft X-ray absorption spectroscopy (NEXAFS) KW - Biaxially streched poly(ehtylene terephthalate) KW - Oxygen DC plasma treatment KW - Metallization with chromium PY - 1997 SN - 0032-3861 SN - 1873-2291 VL - 38 IS - 8 SP - 2005 EP - 2010 PB - Springer CY - Berlin AN - OPUS4-6998 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Wigant, L. A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Wittrich, H. T1 - Corona, spark and combined UV and ozone modification of polymer films WeBP23 N2 - Different types of plasma, irradiative and chemical activation were compared in terms of surface functionalization. Corona and spark jet plasmas are characterized by low gas temperatures and high rates in surface modification. UV irradiation in the presence of ozone does not involve any particle bombardment and acts only by enhanced photooxidative processes. Although ion implantation can be avoided, this method is not free of radiative damage in both the surface-near region and the bulk of polymers. Furthermore, its functionalization rate is low. In relation to low-pressure O2 plasma modification, all treatments mentioned here have a low efficiency in adhesion promotion due to oxidative degradation of macromolecules and formation of molecular debris known as the ''weak boundary layer''. PY - 1998 DO - https://doi.org/10.1016/S0257-8972(97)00318-6 SN - 0257-8972 VL - 98 IS - 1 SP - 879 EP - 885 PB - Elsevier Science CY - Lausanne AN - OPUS4-7000 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian ED - Scheyrer, P. T1 - Vergleich der Wirksamkeit verschiedener Normal- und Niederdruckplasmen bei der Vorbehandlung von Kunststoffen T2 - Seminar Beschriften und vollflächiges Dekorieren von Kunststoffoberflächen CY - Würzburg, Deutschland DA - 1999-03-30 PY - 1995 SP - 14 Seiten PB - Süddeutsches Kunststoffzentrum CY - Würzburg AN - OPUS4-7002 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian T1 - Plasmabehandlung von Polymeren PY - 1997 SN - 0001-8198 SN - 0943-1454 VL - 41 IS - 1-2 SP - 28 EP - 33 PB - Vieweg CY - Wiesbaden AN - OPUS4-7003 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Kühn, Gerhard A1 - Mix, Renate ED - D'Agostino, R. T1 - Polymer Surface Modification with Monofunctional Groups of Different Type and Density T2 - 16th International Symposium on Plasma Chemistry ; ISPC-16 CY - Taormina, Italy DA - 2003-06-22 PY - 2005 SN - 3-527-40487-2 SP - 3 EP - 21 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-7019 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Friedrich, Jörg Florian A1 - Wigant, L. A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Erdmann, J. A1 - Gorsler, H.-V. T1 - Oberflächenvorbehandlung von Polypropylen in elektrischen Entladungen PY - 1995 SN - 0590-8450 VL - 1 SP - 123 EP - 127 PB - Verl. Coating Thomas CY - St. Gallen AN - OPUS4-7005 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Wigant, L. A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Wittrich, H. A1 - Prescher, D. ED - Mittal, K. L. T1 - Barrier properties of plasma-modified polypropylene and polyethyleneterephthalate T2 - International Symposium on Polymer Surface Modification: Relevance to Adhesion CY - Las Vegas, NV, USA DA - 1993-11-03 KW - Plasma fluorination of polymers KW - Deposition of fluorine-containing plasma polymers KW - Barrier formation against solvent permeation KW - Permeation mechanism of solvent mixtures PY - 1996 SN - 90-6764-201-0 VL - 1 SP - 121 EP - 136 PB - VSP CY - Utrecht AN - OPUS4-7006 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Gross, Thomas A1 - Rohrer, P. A1 - Saur, W. A1 - Erdmann, J. A1 - Gorsler, H.-V. ED - Mittal, K. L. T1 - The improvement in adhesion of polyurethane-polypropylene composites by short-time exposure of polypropylene to low and atmospheric pressure plasmas KW - Polyurethane-polypropylene adhesion KW - Low pressure plasma pretreatment KW - Atmospheric pressure plasma treatment KW - Short-time exposure KW - Relevance of functional groups to adhesion KW - Molecular orientation at polymer surfaces PY - 1996 SN - 90-6764-201-0 SP - 49 EP - 72 PB - VSP CY - Utrecht AN - OPUS4-7007 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -