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Paper des Monats
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Eingeladener Vortrag
- nein (99)
An AFM-ESEM Hybride
(2003)
Thin polyamide-6 films were exposed to fluorine gas and analysed with photoelectron and infrared spectroscopies. Fluorine cleaves the amide CN bond resulting in the formation of the COOH and NF2 terminal groups. This is evident from large shifts in the N1s binding energy (+5 eV) and C=O stretching frequency (~80 cm-1), appearance of ester oxygen in the XPS spectra, as well as by the 19F nmr spectra of volatile products consistent with a terminal NF2 group.
Dynamic Plowing Lithography
(2001)
The Normal Force Modulation as a method for Studying the Interphase of Fibre Reinforced Polymer
(1998)
Laminates of carbon fiber reinforced plastic (CFRP), which are manufactured by injection technology, are reinforced with boehmite particles. This doping strengthens the laminates, whose original properties are weaker than those of prepregs. Besides the shear strength, compression strength and the damage tolerance, the mode of action of the nanoparticles in resin and in CFRP is also analyzed. It thereby reveals that the hydroxyl groups and even more a taurine modification of the boehmites' surface alter the elementary polymer morphology. Consequently a new flow and reaction comportment, lower glass transition temperatures and shrinkage, as well as a changed mechanical behavior occur. Due to a structural upgrading of the matrix (higher shear stiffness, reduced residual stress), a better fiber-matrix adhesion, and differing crack paths, the boehmite nanoparticles move the degradation barrier of the material to higher loadings, thus resulting in considerably upgraded new CFRP.
For the first time, we report the direct observation of the nanoscale adsorption and desorption of 2,4,6-trinitrophenol (TNP) molecules on the crystal surface during atomic force microscopy scanning. Our results reveal the position instability of TNP molecules at the border of molecular layers under normal ambient conditions. The observed phenomena are of great interest for exploring the origin of hot-spot generation on the surface of energetic materials. On the basis of the explored properties of TNP crystal, a plausible mechanism of hot-spot formation upon weak initiation at the nanoscale is proposed.
Analytical and numerical analysis of imaging mechanism of dynamic scanning electron microscopy
(2012)
The direct observation of small oscillating structures with the help of a scanning electron beam is a new approach to study the vibrational dynamics of cantilevers and microelectromechanical systems. In the scanning electron microscope, the conventional signal of secondary electrons (SE, dc part) is separated from the signal response of the SE detector, which is correlated to the respective excitation frequency for vibration by means of a lock-in amplifier. The dynamic response is separated either into images of amplitude and phase shift or into real and imaginary parts. Spatial resolution is limited to the diameter of the electron beam. The sensitivity limit to vibrational motion is estimated to be sub-nanometer for high integration times. Due to complex imaging mechanisms, a theoretical model was developed for the interpretation of the obtained measurements, relating cantilever shapes to interaction processes consisting of incident electron beam, electron–lever interaction, emitted electrons and detector response. Conclusions drawn from this new model are compared with numerical results based on the Euler–Bernoulli equation.
Energetische Materialien enthalten gespeicherte chemische Energie. Diese potentielle Energie kann bei Zündung schlagartig als Strahlungsenergie und Druckerhöhung freigesetzt werden. Nanoskalige Komponenten erhöhen zusätzlich die innere Energie des Materials um den Beitrag der Oberflächenenergie und verbessern die chemische Umsetzung durch bessere Durchmischung. Die hot-spot-Theorie zur Zündung von Explosivstoffen kombiniert mechanische Stimulation und einer dabei zu erreichenden Schwellwert-Energie mit der Temperatur. Wird die Energie zum exothermen Bindungsbruch etwa beim Reibvorgang erreicht entsteht auf der molekularen Skala ein hot-spot. Der Stoff explodiert, wenn der hot-spot ausreichend lange besteht, sich verstärkt und nicht durch Energiedissipation (Festkörperschallausbreitung, Wärmediffusion) verzehrt wird.
Rasterkraftmikroskopie (AFM atomic force microscopy) dient nicht nur zur bildgebenden Vermessung der Topographie und der mechanischen Eigenschaften, sondern kann auch zur gezielten Veränderung der Oberflächen verwendet werden. Solche lithographischen Verfahren bedienen sich im AFM-Kontaktmodus (Scratching Lithography) direkt der Reibung, im hochfrequenten intermittierenden Kontaktverfahren realisiert man einen vibrierenden Kontaktes (Dynamic Plowing Lithography), der beim Eindringen in eigenen Indentationseindruck reibt. In beiden Fällen überträgt man durch Kombination einer Scherbewegung mit einer Variation des Kontaktdrucks Energie auf die Oberfläche, was nachweislich zum chemischen Bindungsbruch z.B. auf Polymeroberflächen führt. Zwei kristalline Explosivstoffe werden untersucht und sowohl dissipative Effekte als auch die Generierung eines hot-spots demonstriert.
The ultra–precision cutting of steel materials is possible but needs modifications of machine tools or the workpiece material. One approach of actual research is the development of cutting materials that gives the opportunity for direct cutting of surfaces with ultra–precision quality. Binderless–cBN is here one of the most promising materials. The paper shows results of experimental studies with binderless–cBN as cutting material while turning stainless steel. Various investigations were carried out to determine the wear mechanisms. Furthermore, measurements are shown regarding the surface quality. The achieved results show the high potential ofbinderless–cBN as cutting material for the machining of steel.
Femtosecond time-resolved microscopy has been used to analyze the structural transformation dynamics (melting, ablation, and solidification phenomena) induced by single intense 130 fs laser pulses in single-crystalline (100)-indium phosphide wafers in air on a time scale from ~100 fs up to 8 ns. In the ablative regime close to the ablation threshold, transient surface reflectivity patterns are observed by fs microscopy on a ps to ns time scale as a consequence of the complex spatial density structure of the ablating material (dynamic Newton fringes). At higher fluences, exceeding six times the ablation threshold, optical breakdown causes another, more violent ablation regime, which reduces the energy deposition depth along with the time of significant material removal. As a consequence, ablation lasts longer in a ring-shaped region around the region of optical breakdown. This leads to the formation of a crater profile with a central protrusion. In the melting regime below the ablation threshold, the melting dynamics of indium phosphide has been quantified and subsequent superficial amorphization has been observed upon solidification on the ns time scale leading to amorphous layer thicknesses of the order of a few tens of nanometers.
The pyrolysis and fire behavior of glass-fiber reinforced poly(butylene terephthalate) (PBT/GF) with two different metal phosphinates as flame retardants in combination with and without melamine cyanurate (MC) were analyzed by means of thermogravimetry, thermogravimetry coupled with infrared spectroscopy, flammability, and cone calorimeter tests as well as scanning electron microscopy/energy dispersive X-ray spectroscopy and X-ray fluorescence spectroscopy. In PBT/GF, dosages of 13-20% of the halogen-free flame retardant aluminum phosphinate or aluminum phosphinate in combination with MC fulfill the requirements for electrical engineering and electronics applications (UL 94 = V-0; LOI > 42%), whereas the use of the same amount of zinc phosphinate or zinc phosphinate in combination with MC does not improve the fire behavior satisfactorily (UL 94 = HB; LOI = 27-28%). The performance under forced flaming conditions (cone calorimeter) is quite similar for both of the metal phosphinates. The use of aluminum and zinc salts results in similar flame inhibition predominantly due to the release of the phosphinate compounds in the gas phase. Both metal phosphinates and MC interact with the polymer changing the decomposition characteristics. However, part of the zinc phosphinate vaporizes as a complete molecule. Because of the different decomposition behavior of the metal salts, only the aluminum phosphinate results in a small amount of thermally stable carbonaceous char. In particular, the aluminum phosphinate-terephthalate formed is more stable than the zinc phosphinate-terephthalate. The small amount of char has a crucial effect on the thermal properties and mechanical stability of the residue and thus the flammability.
Modulated lateral force microscopy: an AFM tool for analysis and modification of polymer surfaces
(2007)
Modulated lateral force microscopy: An AFM tool for analysis and modification of polymer surfaces
(2007)
Rasterkraftmikroskopische Verfahren zur Beschreibung der Grenzflächen in Polymer-Kompositwerkstoffen
(2010)
Von makroskopischen Fragestellungen und mikroskopischen Untersuchungsmethoden in der Tribologie
(2010)
Modulated lateral force microscopy: an AFM tool for analysis and modification of polymer surfaces
(2007)
Para-hexaphenylene (p-6P) molecules exhibit a characteristic photoinduced reaction (bleaching) resulting in a decrease in luminescence intensity upon UV light exposure, which could render the technological use of the nanofibers problematic. In order to investigate the photoinduced reaction in nanofibers, optical bleaching experiments have been performed by irradiating both pristine and coated nanofibers with UV light. Oxide coating materials (SiOx and Al2O3) were applied onto p-6P nanofibers. These treatments caused a reduction in the bleaching reaction but in addition, the nanofiber luminescence spectrum was significantly altered. It was observed that some polymer coatings [a statistical copolymer of tetrafluoroethylene and 2,2-bis-trifluoromethyl-4,5-difluoro-1,3-dioxole, P(TFE-PDD), and poly(methyl methacrylate), PMMA] do not interfere with the luminescence spectrum from the p-6P but are not effective in stopping the bleaching. Bilayer coatings with first a polymer material, which should work as a protection layer to avoid modifications of the p-6P luminescence spectrum, and second an oxide layer used as oxygen blocker were tested and it was found that a particular bilayer polymer/oxide combination results in a significant reduction in bleaching without affecting significantly the emission spectrum from the nanofibers.