Filtern
Erscheinungsjahr
- 2003 (147) (entfernen)
Dokumenttyp
Referierte Publikation
- ja (147) (entfernen)
Schlagworte
- Raman spectroscopy (4)
- Reference materials (4)
- Radar (3)
- XPS (3)
- Amino group (2)
- Aza-enamines (2)
- Bioceramics (2)
- Ceramics (2)
- Concrete (2)
- Crystal structure (2)
Adhesion and other mechanical behaviour of coatings is at present routinely tested in industry and research organisations using the scratch test. The test has been the subject of a European Standard prEN 1071-3:2000 established by the European Standards Committee CEN TC184 WG5. A previous European project on the development and validation of test methods for thin hard coatings—FASTE—revealed that uncertainties in the Rockwell C stylus tip shape represent a major source of error for the scratch-test method. Therefore a follow-up project—REMAST—was started to develop and certify a reference material as a quality control tool for the testing and qualification of scratch-test instruments. In addition, a considerable effort was devoted to improve the scratch stylus manufacturing process. This paper presents the results of the REMAST project. During a feasibility study, two candidate materials—titanium nitride (TiN) and diamond-like carbon (DLC) coatings both on high speed steel substrates—were evaluated. Because of the lower sensitivity to styli tip shape variations and higher data scatter observed for the TiN coating, DLC was chosen as the reference material to be certified. One thousand samples were produced, as well as qualified styli to carry out the certification campaign, including homogeneity and stability testing. Nine independent laboratories were involved in the certification exercise, and the data were statistically analysed to obtain the certified critical load values and their uncertainty ranges. A certified reference material BCR-692 is available for verification purposes. This presents three repeatable failure events at certified critical load intervals and can provide a good indication of overall scratch-test instrument performance, including stylus condition and calibration. It is also useful as a diagnostic tool, providing a means of sensitive monitoring of machine and stylus performance over extended periods. Considerable improvement of the quality of scratch styli was achieved by the strict control of all manufacturing steps.
Bench scale performance based cone calorimeter investigations were conducted on glass fibre reinforced polyamide 66 (PA-66) and high impact polystyrene (HIPS) materials. Red phosphorus and magnesium hydroxide were used as fire retardants. Dilution, heat sink, barrier and charring mechanisms are considered to be active in the condensed phase. Dilution, cooling and flame poisoning mechanisms are discussed for the gas phase. Cone calorimeter data are used to give a comprehensive fire behaviour assessment in terms of the propensity to cause a quick growing fire and of the propensity to cause a fire of long duration. The external heat flux is varied between 30 and 75 kW/m2 so that the results for combustion behaviour and flame retardancy, respectively, are valid for different fire scenarios and fire tests. Results on the intrinsic contribution of the steady heat release rate per unit area reveal information about the flammability behaviour. UL 94 results are predicted in close correspondence to UL 94 experiments.
Low-pressure gas-discharge plasmas are widely used for polymer surface functionalization on industrial scale. For biomaterial applications, the density and selectivity of the functionalization are of particular importance, because functional groups control the immobilization of biomolecules. Therefore, surface modification of biomaterials is a challenging task for low-pressure plasma technique. Plasma processes have been successfully applied to various polymer types in order to generate multifunctional surfaces. This paper discusses the present state and the prospects of non-coating plasma processes to generate mono functional surfaces of controlled amino group density. Such surfaces appear most desirable for many applications. The results of various microwave- and radio-frequency- excited plasma processes reported in the literature are reviewed and compared to a sequence of experiments that was conducted in a UHV reaction environment. Non-thermal plasmas are especially well suited for thermally damageable polymers. The effect of hydrogen admixture to discharges in nitrogen and ammonia is discussed in detail. The optimization of process parameters lead to highly selective amino functionalization of high density. The selectivity reached 100% -NH2/N at a surface density of amino groups of 3% -NH2/C.
Pulsed and cw microwave plasma excitation for surface functionalization in nitrogen-containing gases
(2003)
Results are presented of polymer surface functionalization processes in pulsed and continuous wave (cw) microwave-excited plasmas in nitrogen-containing gases under admixture of hydrogen. A maximum selectivity of 100% for amino groups with respect to all nitrogen functional groups (NH2/N) was obtained in cw microwave (MW) plasmas either for very short treatment durations below 100 µs in pure NH3, or within approximately 10 s in hydrogen-rich nitrogen-containing plasmas. The amino and overall nitrogen surface densities, NH2/C and N/C, reach up to 3.5% and 35%, respectively. Post plasma processes of functionalized polymers are discussed in the light of monofunctionalization. Down to pulse duration of 1 ms, plasma decomposition rates of NH3, determined by infrared absorption spectroscopy, are found to scale linearly with the duty cycle. In this regime, the main effect of a duty cycle variation in pulsed NH3 plasmas on surface functionalization can be interpreted to result from changes in the concentration of the dominant stable species in the gas phase, NH3, N2 and H2, which are activated by subsequent plasma pulses. With increasing duty cycle, NH3 decomposition to N2 and 3H2 more and more dominates over the supply of fresh NH3. The nitrogen-removing role of hydrogen in the plasma is discussed in detail, whereas the role of the numerous transient nitrogen-containing species remains to be studied in the future.
Numerous polycondensations of isosorbide and suberoyl chloride or other aliphatic dicarboxylic acid dichlorides were performed with pyridine as a catalyst and HCl acceptor. The reaction conditions were varied to optimize both the molecular weight and the fraction of cyclic oligo- and polyesters. Furthermore, we attempted to obtain the cyclic monomer by catalyzed back-biting degradation of the molten cyclic polyesters above 220 °C in vacuo. The polyesters were characterized by viscosity and size exclusion chromatographic measurements as well as matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. In selected cases, mixtures of linear and cyclic polyesters were treated with a hot solution of partially methylated ß-cyclodextrin in methanol. This treatment allowed for a selective extraction of the linear chains up to approximately 5000 Da.
New thermography systems enable the application of active investigation techniques, i.e. the observation of the cooling down process after heating the surface of a structure under investigation. Defects like voids in concrete having a different thermal diffusivity in comparison to the bulk material are visualised by different surface temperatures. The differences between temperature transient curves above sound regions and above inhomogeneities are expected to include information about the defect parameters.
Experimental investigations with impulse thermography and radar on a concrete test specimen containing voids were analysed. Radar was used to determine the depth of the voids. The influence of size and depth of the voids on the temperature transient curves was studied for different heating times. The transient curves were also fitted with a simple semi-empirical model.
Textile, aluminium and polyethylene used as components in laser protection curtains were investigated with respect to their ablation behaviour. Employing 33-fs pulses (800 nm wavelength, 1 kHz repetition rate), ex situ geometrical measurements of the ablation cavities and in situ acoustic investigations with a microphone were performed to determine the ablation thresholds in the single- and multi-pulse cases. The acoustical method proved advantageous for complex surface morphologies and/or single laser pulse interactions. Incubation phenomena can be observed for all the materials studied. Technically relevant multi-pulse ablation thresholds are presented and are compared with the single-pulse (1-on-1) irradiation.
Ablation experiments employing Ti:sapphire laser pulses with durations from 30 to 340 fs (centre wavelength 800 nm, repetition rate 1 kHz) were performed in air. Absorbing filters (Schott BG18 and BG36) served as targets. The direct focusing technique was used under single- and multi-pulse irradiation conditions. Ablation threshold fluences were determined from a semi-logarithmic plot of the ablation crater diameter versus laser fluence. The threshold fluence decreases for a shorter pulse duration and an increasing number of pulses. The multi-pulse ablation threshold fluences are similar to those of undoped glass material (~1 J cm-2). That means that the multi-pulse ablation threshold is independent on the doping level of the filters. For more than 100 pulses per spot and all pulse durations applied, the threshold fluence is practically constant. This leads to technically relevant ablation threshold values.
Glasses of the compositional series of 50PbOyB2O3(50-y)P2O5xTiO2 (with x=016) have been prepared and characterized by the determination of density, molar volume, glass transition temperature, dilatation softening temperature, thermal and chemical durability. Structural changes were evaluated from the studies by 31P and 11B MAS NMR, Raman and infrared spectroscopy. Molar volume of the glasses decreases and the glass transition temperature increases with increasing additions of TiO2. 31P MAS NMR spectra revealed that titanate units enter phosphate chains decreasing the number of Q2 units and increasing the number of Q1 units. This result is confirmed by the observed changes in the Raman and infrared spectra of the TiO2-doped glasses.