TY - JOUR A1 - Natte, Kishore A1 - Behnke, Thomas A1 - Orts Gil, Guillermo A1 - Würth, Christian A1 - Friedrich, Jörg Florian A1 - Österle, Werner A1 - Resch-Genger, Ute T1 - Synthesis and characterisation of highly fluorescent core-shell nanoparticles based on Alexa dyes N2 - Current and future developments in the emerging field of nanobiotechnology are closely linked to the rational design of novel fluorescent nanomaterials, e.g. for biosensing and imaging applications. Here, the synthesis of bright near infrared (NIR)-emissive nanoparticles based on the grafting of silica nanoparticles (SNPs) with 3-aminopropyl triethoxysilane (APTES) followed by covalent attachment of Alexa dyes and their subsequent shielding by an additional silica shell are presented. These nanoparticles were investigated by dynamic light scattering (DLS), transmission electron microscopy (TEM) and fluorescence spectroscopy. TEM studies revealed the monodispersity of the initially prepared and fluorophorelabelled silica particles and the subsequent formation of raspberry-like structures after addition of a silica precursor.Measurements of absolute fluorescence Quantum yields of these scattering particle suspensions with an integrating sphere setup demonstrated the influence of dye labelling density-dependent fluorophore Aggregation on the signaling behaviour of such nanoparticles. KW - Silica KW - Alexa dyes KW - Fluorescent particles KW - Quantum yields KW - Nanoparticles KW - Protective shell KW - Nanobiotechnology PY - 2012 DO - https://doi.org/10.1007/s11051-011-0680-9 SN - 1388-0764 SN - 1572-896X VL - 14 IS - 2 SP - 680-1 - 680-10 PB - Kluwer CY - Dordrecht AN - OPUS4-25872 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hanelt, Sven A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus T1 - UV spectrometric indirect analysis of brominated MWCNTs with UV active thiols and an alkene-reaction kinetics, quantification and differentiation of adsorbed bromine and oxygen N2 - Indirect UV-absorption spectrometry was shown to be a valuable tool for chemical characterization of functionalized carbon nanotubes (CNTs). It complements data from X-ray photoelectron spectroscopy (XPS) or FTIR analysis since it helps to clarify the type and concentration of functional groups. The principles of indirect application of UV-spectrometry and its mathematical interpretation are discussed. Their facile application, together with their adequate sensitivity and high flexibility, make UV-absorption-based approaches a valuable alternative to fluorescence spectrometry. Here, the approach was applied to the chemical analysis of oxidizing substances on CNTs. For this, pristine CNTs of low but finite oxygen content as well as brominated CNTs were analyzed by reaction in suspension with UV-active thiol reagents and a styrene derivative. It was shown that carefully selected reagents allow differentiation and quantification of bromine and generally oxidizing entities like oxygen. For brominated CNTs, it was shown that physisorbed bromine may dominate the overall bromine content. KW - Carbon nanotubes KW - CNTs KW - UV-spectrometry KW - Bromination KW - Thiols KW - Mercaptans KW - Disulfides KW - Quantification KW - Kinetics PY - 2013 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-289077 DO - https://doi.org/10.3390/ma6083035 SN - 1996-1944 VL - 6 IS - 8 SP - 3035 EP - 3063 PB - MDPI CY - Basel AN - OPUS4-28907 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ramanujam, Maalolan A1 - Wachtendorf, Volker A1 - Purohit, Purv A1 - Mix, Renate A1 - Schönhals, Andreas A1 - Friedrich, Jörg Florian T1 - A detailed dielectric relaxation spectroscopy study of artificial UV weathered low density polyethylene N2 - Artificial weathering of LDPE under dry conditions (<10% of relative humidity) by UV radiation was monitored by dielectric spectroscopy. For an apolar polymer like LDPE, dielectric study yields Information about the change in structure and dynamics of the system. The fluctuations of the polar groups which are generated as a result of photooxidation such as carbonyl groups can be monitored as characteristic relaxation processes like the αc or β mode. The dielectric loss characterized by typical dielectric parameters like the activation energy and dielectric strength are strongly dependent upon changes induced by photooxidation in the amorphous and crystalline domains. This paper discusses in detail how the foil reached its mechanical disintegration. It was found that initial stages of weathering induce chain scission and/or crosslinking in the amorphous domains of the polymer and the motional processes in the crystalline regions are not affected. After this induction period, an increase in the degree of crystallization was observed by employing differential calorimetry. The increasing crystallinity is considered as one of the reasons for embrittlement which finally leads to the complete loss of the structural integrity. KW - Artificial weathering KW - UV radiation KW - Dielectric relaxation KW - LDPE PY - 2012 DO - https://doi.org/10.1016/j.tca.2011.12.003 SN - 0040-6031 SN - 1872-762X VL - 530 SP - 73 EP - 78 PB - Elsevier CY - Amsterdam AN - OPUS4-25547 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Altmann, Korinna A1 - Schulze, Rolf-Dieter A1 - Hidde, Gundula A1 - Friedrich, Jörg Florian T1 - Elektrospray-Ionisation (ESI) - Lochfreie elektrophoretische Abscheidung von ultra-dünnen Polymerschichten N2 - Die Elektrospray-Ionisations (ESI)-Vernebelung von Polymerlösungen wird analytisch zur massenspektrometrischen Bestimmung der Molmassen von Makromolekülen genutzt. Dabei werden die Polymermoleküle nach einem speziellen Mechanismus im Hochspannungsfeld unter Normaldruckbedingungen vereinzelt und in das Massenspektrometer überführt. Dieser Prozeß kann auch zur flächigen Abscheidung einzelner Polymermoleküle genutzt werden. Die Struktur und Zusammensetzung sowie die Molmassenverteilung der Polymere bleiben dabei erhalten. Schichten polarer oder ionischer Polymere der Dicke einer Quasi-Monolage bis hin zu mehreren 100 Nanometern können abgeschieden werden. Erwähnenswert ist, daß der ESI-Prozeß zu den elektrophoretischen Verfahren gehört, was die Ausbildung lochfreier Schichten auf elektrisch leitenden Substraten nicht nur auf der der Spraydüse zugewandten Seite ermöglicht, sondern auch auf der abgeschatteten Rückseite. Dieses Verhalten wurde zur vollständigen ESI-Umhüllung von dichtgepackten Kohlenstoff-Faser-Bündeln mit haftvermittelnden Polymerschichten ausgenutzt. PY - 2011 DO - https://doi.org/10.1002/vipr.201100471 SN - 0947-076X SN - 1522-2454 VL - 23 IS - 6 SP - 17 EP - 23 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-25392 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Altmann, Korinna A1 - Schulze, Rolf-Dieter A1 - Friedrich, Jörg Florian T1 - Polymer deposition morphology by electrospray deposition - Modifications through distance variation N2 - Electrospray deposition (ESD) of highly diluted polymers was examined with regard to the deposited surface structure. Only the flight distance (flight time) onto the resulting deposited surface was varied from 20 to 200 mm. An apparatus without any additional heating or gas flows was used. Polyacrylic acid (PAA) and polyallylamine (PAAm) in methanol were deposited on Si wafers. The polymer layers were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, derivatization reactions and Fourier transform infrared spectroscopy using a grazing incidence unit. SEM images illustrated the changing structures of PAA and PAAm. For PAA the deposited structure changed from a smooth film (20 mm) to a film with individual droplets on the coated surface (100 mm and 200 mm), while for PAAm individual droplets can be seen at all distances. The ESD process with cascades of splitting droplets slows down for PAA after distances greater than 40 mm. In contrast, the ESD process for PAAm is nearly stopped within the first flight distance of 20 mm. Residual solvent analysis showed that most of the solvent evaporated within the first 20 mm capillary-sample distance. KW - Electrospray ionization KW - Electrospray deposition KW - Ultra-thin layers KW - Capillary-sample distance KW - Residual solvent PY - 2014 DO - https://doi.org/10.1016/j.tsf.2014.06.020 SN - 0040-6090 VL - 564 SP - 269 EP - 276 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-31252 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Altmann, Korinna A1 - Schulze, Rolf-Dieter A1 - Hidde, Gundula A1 - Friedrich, Jörg-Florian T1 - Electrospray ionization for deposition of ultra-thin polymer layers – principle, electrophoretic effect and applications N2 - Nebulizing of polymer solutions, in a high-voltage field under atmospheric conditions by electrospray ionization (ESI), is a comfortable way to deposit ultra-thin layers of polar or ionic polymers onto any conductive substrate materials. The substrate is grounded and the polymer solution is sprayed through a powered capillary. The formed charged droplets shrink by solvent evaporation during their way to the grounded substrate, the charges close ranks and the droplets collapse consecutively by charge repulsion, thus forming finally charged single macromolecules. After their discharging at the grounded substrate, an ultrathin ‘quasi-monomolecular’ polymer layer is formed. It could be shown by imaging of scratches through the polymer layer by atomic force microscopy that the deposited polymer layers are dense at a thickness of about 10 nm. Carbon fibre bundles were coated with poly (allylamine) (PAAm) or poly(acrylic acid) (PAA) as potential adhesion-promoting layers in fibre–polymer composites. The polymer deposition is self-inhibiting after formation of a continuous coverage of about 200 nm for PAAm and 30 nm for PAA as result of surface charging. Continuous deposition onto such isolating layers or polymers without charging can be achieved by using current of alternating polarity. The film formation is self-healing because of the electrophoretic effect, i.e. the ion discharging occurs preferentially at noncoated areas. This electrophoretic effect of ESI was demonstrated by completely enwrapping all the carbon fibres of the roving within a distance of about 100 μm far from its outside and also at the backside of the fibre bundle with about 80% of the topside coverage, as measured by X-ray photoelectron spectroscopy and visualized using scanning electron microscopy. KW - Complete enwrapping of fibres KW - Ultra-thin polymer layers KW - Self-healing KW - Electrospray deposition KW - Carbon fibres KW - Electrophoretic effect PY - 2012 DO - https://doi.org/10.1080/01694243.2012.727170 SN - 0169-4243 VL - 27 IS - 9 SP - 988 EP - 1005 PB - Taylor & Francis CY - London AN - OPUS4-42631 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Weidner, Steffen A1 - Kühn, Gerhard A1 - Decker, Renate A1 - Roessner, D. A1 - Friedrich, Jörg Florian T1 - Influence of Plasma Treatment on the Molar Mass of Poly(ethylene terephthalate) Investigated by Different Chromatographic and Spectroscopic Methods N2 - The influence of different types of low and atmospheric pressure plasma on poly(ethylene terephthalate) (PET) has been studied in terms of changes in molar mass and molar mass distribution. Apart from a variation of plasma gases (oxygen, helium) different types of plasma (microwave, radio frequency, corona discharge) were used for the plasma surface modification. The changes in molar mass and types of functional end groups of lower molar mass products were investigated by means of matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOFMS), whereas the high-molar mass fraction was analyzed by means of size-exclusion chromatography (SEC). The formation of crosslinked products during exposure to a helium plasma, which emits preponderately energy-rich and intense ultraviolet radiation, was proved by means of thermal field-flow fractionation (ThFFF). This method combined with a multiangle laser light scattering (MALLS) detector allows detection of weakly crosslinked polymers and microgels. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1639-1648, 1998 KW - Poly(ethylene terephthalate) KW - PET KW - Plasma PY - 1998 UR - http://www3.interscience.wiley.com/cgi-bin/abstract/36482/ABSTRACT DO - https://doi.org/10.1002/(SICI)1099-0518(19980730)36:10<1639::AID-POLA17>3.0.CO;2-H SN - 0360-6376 SN - 0887-624X VL - 36 IS - 10 SP - 1639 EP - 1648 PB - Wiley CY - Hoboken, NJ AN - OPUS4-6989 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hanelt, Sven A1 - Friedrich, Jörg Florian A1 - Orts Gil, Guillermo A1 - Meyer-Plath, Asmus T1 - Study of Lewis acid catalyzed chemical bromination and bromoalkylation of multi-walled carbon nanotubes N2 - Chemical functionalization of carbon nanotubes (CNT) with nucleophiles requires introduction of electrophilic reactive sites on the CNTs. This can, for instance, be accomplished by the chemical bromination procedure with elemental bromine and a set of Lewis acids (BBr3, BF3 × Et2O, AlBr3, FeBr3, ZnBr2, TiBr4, SiBr4, SnBr4, VBr3) or a radical starter like dibenzoylperoxide (DBPO) in appropriate solvents at varied temperature. The present approach to electrophilic sites relies on the well-known electrophilic aromatic substitution or addition of bromine with aromatic structural units. In addition to the use of bromine, the introduction of haloalkyl groups was also investigated here using bis-electrophiles or haloalcohols and Brønsted acids. The advantages and drawbacks of the studied reaction conditions, the obtained degree of bromination as analyzed by X-ray photoelectron spectroscopy (XPS) and the amount of introduced bromine that can be substituted by a nucleophile are presented and discussed. KW - Carbon nanotubes KW - Bromierung KW - Lewis Säure KW - Bromalkylierung KW - CNT PY - 2012 DO - https://doi.org/10.1016/j.carbon.2011.11.009 SN - 0008-6223 SN - 1873-3891 VL - 50 IS - 3 SP - 1373 EP - 1385 PB - Pergamon Press CY - New York, NY AN - OPUS4-25207 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Koprinarov, Ivaylo A1 - Weidner, Steffen A1 - Kühn, Gerhard ED - Nowack, H. T1 - Wechselwirkungen zwischen plasmamodifizierten Polymeroberflächen und Metallen T2 - 5. Internationale Fachtagung - ND-Plasma-Technologie CY - Duisburg, Deutschland DA - 1997-09-22 PY - 1997 VL - 5 SP - 1(?) EP - 17(?) PB - Print-Service CY - Mülheim AN - OPUS4-6995 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Weidner, Steffen A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Krüger, Ralph-Peter A1 - Friedrich, Jörg Florian T1 - Determination of chemical and molecular-weight distributions of heterogeneous polymers by means of MALDI-MS coupled with chromatography T2 - 219th ACS national meeting CY - San Francisco, CA, USA DA - 2000-03-26 PY - 2000 SN - 0032-3934 VL - 41 IS - 1 SP - 655 EP - 656 PB - American Chemical Society CY - Newark, NJ AN - OPUS4-2169 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kühn, Gerhard A1 - Ghode, Archana A1 - Weidner, Steffen A1 - Retzko, Iris A1 - Unger, Wolfgang A1 - Friedrich, Jörg Florian ED - Mittal, K. L. T1 - Chemically well-defined surface functionalization of polyethylene and polypropylene by pulsed plasma modification followed by grafting of molecules T2 - 2nd International Symposium on Polymer Surface Modification: Relevance to Adhesion CY - Newark, NJ, USA DA - 1999-05-24 KW - Plasma modification KW - Chemical conversion of functional groups KW - Spacers KW - Polypropylene KW - Polyethylene PY - 2000 SN - 90-6764-327-0 VL - 2 SP - 45 EP - 64 PB - VSP CY - Utrecht AN - OPUS4-6975 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Gerstung, Vanessa A1 - Mix, Renate A1 - Kühn, Gerhard A1 - Weidner, Steffen ED - d'Agostino, R. T1 - Pulsed plasma initiated homo- and copolymerisation - molar masses 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 - OPUS4-2710 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Friedrich, Jörg Florian T1 - Beiträge zur Charakterisierung von synthetischen Si-Polymeren durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-MS T2 - DFG-Symposium zum Schwerpunktprogramm "Silicium-Chemie" CY - Werfenweng, Österreich DA - 2000-09-27 PY - 2000 AN - OPUS4-2251 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Falkenhagen, Jana A1 - Friedrich, Jörg Florian A1 - Schulz, Günter A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Weidner, Steffen T1 - Liquid Adsorption Chromatography near Critical Conditions of Adsorption coupled with Matrix-assisted Laser Desorption/Ionization Mass Spectrometry N2 - Chemical heterogeneities and molecular weight distributions of poly(ethylene oxide) (PEO)-co-polymethylene (PM) model oligomers, which are relevant to the synthesis of commonly used tensides, were investigated. For analytical characterization, the well-known principle of liquid adsorption chromatography at 'critical conditions' (LACCC) was modified. Near the critical conditions of adsorption of the PEO unit, e.g., at slight adsorption conditions of PM, the copolymers could be separated according to their PM chain length. The eluates were separated and single fractions of each peak were continuously transferred onto the MALDI target by means of a commercially available device. Simultaneously, the MALDI matrix solution was continuously added with a second pump. This procedure offers the possibility of the formation of homogeneous matrix-polymer textures. By MALDI-MS a complete characterization of the chemical composition (PEO and PM chain length) of each peak could be achieved. The obtained MALDI mass spectra of the eluates at different retention times could be used for the molecular weight calibration of the LAC system. In this way, an additional application of SEC, as in conventional 2D-chromatography, was avoided by using the MALDI method as quasi chromatographic separation KW - Liquid adsorption chromatography KW - Matrix-assisted laser desorption KW - Ionization mass spectrometry KW - Coupling methods KW - MALDI PY - 2000 DO - https://doi.org/10.1080/10236660008034644 SN - 1023-666X SN - 1563-5341 VL - 5 SP - 549 EP - 562 PB - Gordon and Breach Publ. CY - Amsterdam AN - OPUS4-2168 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Weidner, Steffen A1 - Just, Ulrich A1 - Wittke, Wolfgang A1 - Rittig, F. A1 - Gruber, F. A1 - Friedrich, Jörg Florian T1 - Analysis of modified polyamide 6.6 using coupled liquid chromatography and MALDI-TOF-mass spectrometry KW - MALDI-TOF-MS KW - Liquid chromatography KW - Coupling methods PY - 2004 SN - 0168-1176 SN - 0020-7381 SN - 1387-3806 SN - 1873-2798 VL - 238 IS - 3 SP - 235 EP - 244 PB - Elsevier CY - Amsterdam AN - OPUS4-6966 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Krüger, Ralph-Peter A1 - Heinemann, M. A1 - Falkenhagen, Jana A1 - Hartmann, A. A1 - Friedrich, Jörg Florian A1 - Fritz, H.-G. ED - Fritz, H. ED - Eisenbach, C. T1 - Charakterisierung biologisch abbaubarer Homo- und Copolyester / Characterisation of biodegradable Homo- and Copolyesters T2 - 19. Stuttgarter Kunststoff-Kolloquium 2005 CY - Stuttgart, Deutschland DA - 2005-03-09 KW - MALDI-TOF-MS KW - Bioabbaubare Polyester KW - Flüssigchromatographie KW - Methodenkopplung KW - Biodegradable polyesters KW - Liquid chromatography KW - Coupling of analytical methods PY - 2005 SN - 3-00-015246-6 SP - 5/P1-1 - 5/P1-9 PB - IKT CY - Stuttgart AN - OPUS4-11767 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wettmarshausen, Sascha A1 - Friedrich, Jörg Florian A1 - Meyer-Plath, Asmus A1 - Kalinka, Gerhard A1 - Hidde, Gundula A1 - Weidner, Steffen T1 - Coating of carbon fibers with adhesion-promoting thin poly(acrylic acid) and poly(hydroxyethylmethacrylate) layers using electrospray ionization N2 - Thin coatings of poly(acrylic acid) (PAA) and poly(hydroxyethylmethacrylate) (PHEMA) were deposited onto carbon fibers by means of the electrospray ionization (ESI) technique in ambient air. These high-molecular weight polymer layers were used as adhesion promoters in carbon fiber–epoxy resin composites. Within the ESI process, the carbon fibers were completely enwrapped with polymer in the upper 10 plies of a carbon fiber roving. As identified with scanning electron microscopy also shadowed fibers in a bundle as well as backsides of fiber rovings were pinhole-free coated with polymers (‘electrophoretic effect'). Under the conditions used, the layers have a granular structure. Residual solvent was absent in the deposit. PAA and PHEMA films did not show any changes in composition and structure in comparison with the original polymers as analyzed by X-ray photo-electron spectroscopy and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Single-fiber pullout tests of coated fibers embedded in epoxy resin showed significantly increased interfacial shear strength. It is assumed that chemical bonds between carbon fiber poly(acrylic acid) and epoxy resin contribute significantly to the improved interactions. KW - Adhesion promotion KW - Thin polymer layers KW - Electrospray ionization (ESI) KW - Carbon fiber–epoxy resin laminates KW - Layer topography PY - 2015 DO - https://doi.org/10.1080/01694243.2015.1040980 SN - 0169-4243 SN - 1568-5616 VL - 29 IS - 15 SP - 1628 EP - 1650 PB - VNU Science Press CY - Utrecht AN - OPUS4-34564 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Weidner, Steffen A1 - Falkenhagen, Jana A1 - Friedrich, Jörg Florian A1 - Krüger, Ralph-Peter A1 - Schulz, Günter A1 - Much, Helmut T1 - Liquid Adsorption Chromatography near Critical Conditions of Adsorption coupled with Matrix-assisted Laser/Ionization Mass Spectrometry T2 - 47th ASMS Conference on Mass Spectrometry and Allied Topics CY - Dallas, TX, USA DA - 1999-06-13 PY - 1999 CY - Dallas, Tex AN - OPUS4-2165 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Friedrich, Jörg Florian A1 - Much, Helmut A1 - Schulz, Günter A1 - Falkenhagen, Jana T1 - Zur Charakterisierung von Si-Polymeren durch Kopplung flüssigchromatographischer Arbeitsweisen mit der MALDI-TOF-MS T2 - DFG-Symposium zum Schwerpunktprogramm "Silicium-Chemie" CY - Bielefeld, Deutschland DA - 1999-05-09 PY - 1999 AN - OPUS4-2239 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Friedrich, Jörg Florian A1 - Schulz, Eckhard A1 - Weidner, Steffen A1 - Kühn, Gerhard T1 - Verbesserungen der mechanischen Festigkeiten von Faser-Polymer-Verbundwerkstoffen durch Vorbehandlung der Fasern im Niederdruckplasma T2 - Vortragsbände des 8. Internationalen Techtextil-Symposiums 1997 CY - Frankfurt am Main, Deutschland DA - 1997-05-12 PY - 1997 VL - 8 SP - 1(?) EP - 16(?) PB - Messe Frankfurt CY - Frankfurt am Main AN - OPUS4-7287 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Friedrich, Jörg Florian A1 - Unger, Wolfgang A1 - Lippitz, Andreas A1 - Koprinarov, Ivaylo A1 - Kühn, Gerhard A1 - Weidner, Steffen A1 - Vogel, Lydia ED - Mittal, K. T1 - Plasma Pretreatment of Polymer Surfaces - Relevance to Adhesion of Metals T2 - 5th Symposium on Metallized Plastics ; 6th Symposium on Metallized Plastics CY - Los Angeles, CA, USA DA - 1996-05-05 PY - 1998 SN - 90-6764-290-8 SP - 271 EP - 293 PB - VSP CY - Utrecht AN - OPUS4-6987 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kühn, Gerhard A1 - Weidner, Steffen A1 - Decker, Renate A1 - Ghode, Archana A1 - Friedrich, Jörg Florian T1 - Selective surface functionalization of polyolefins by plasma treatment followed by chemical reduction N2 - Polymer surfaces can be finished with functional groups upon exposure to a plasma. Species of the plasma gas are attached at surface carbon atoms, forming functional groups of different composition. To produce a modified polymer surface with a high density and homogeneity of hydroxyl groups only, the oxygen-plasma-formed oxygen functional groups were chemically reduced by diborane and LiAlH4 with yields of 10 to 11 OH groups per 100 carbon atoms in the 3 to 5 nm near-surface layer as detected by X-ray photoelectron spectroscopy (XPS). The identification of hydroxyl groups was performed by means of attenuated total reflectance–Fourier transform infrared spectroscopy and XPS. KW - Attenuated total reflectance-Fourier transorm infrared spectroscopy KW - Chemical reduction of functional groups KW - Plasma modification KW - X-ray photoelectron spectroscopy PY - 1999 DO - https://doi.org/10.1016/S0257-8972(99)00232-7 SN - 0257-8972 VL - 116-119 SP - 796 EP - 801 PB - Elsevier Science CY - Lausanne AN - OPUS4-6983 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Friedrich, Jörg Florian T1 - Beiträge zur Charakterisierung von synthetischen Si-Polymeren durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-MS T2 - Incom 2001 - International Symposium on Instrumentalized Analytical Chemistry and Computer Technology CY - Düsseldorf, Deutschland DA - 2001-03-27 PY - 2001 AN - OPUS4-2254 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -