RESUMEN
Femtosecond laser-induced breakdown spectroscopy (fs-LIBS) is employed to detect tiny amounts of mass ablated from macroscopic specimens and to measure chemical images of microstructured samples with high spatial resolution. Frequency-doubled fs-pulses (length 400 fs, wavelength 520 nm) are tightly focused with a Schwarzschild microscope objective to ablate the sample surface. The optical emission of laser-induced plasma (LIP) is collected by the objective and measured with an echelle spectrometer equipped with an intensified charge-coupled device camera. A second fs-laser pulse (1040 nm) in orthogonal beam arrangement is reheating the LIP. The optimization of the experimental setup and measurement parameters enables us to record single-pulse fs-LIBS spectra of 5 nm thin metal layers with an ablated mass per pulse of 100 femtogram (fg) for Cu and 370 fg for Ag films. The orthogonal double-pulse fs-LIBS enhances the recorded emission line intensities (two to three times) and improves the contrast of chemical images in comparison to single-pulse measurements. The size of ablation craters (diameters as small as 1.5 µm) is not increased by the second laser pulse. The combination of minimally invasive sampling by a tightly focused low-energy fs-pulse and of strong enhancement of plasma emission by an orthogonal high-energy fs-pulse appears promising for future LIBS chemical imaging with high spatial resolution and with high spectrochemical sensitivity.
RESUMEN
The properties of natural and synthetic rubber critically depend on the concentration of the vulcanizing system, among others. Sulfur and zinc oxide are typically used as cross-linking and activating agents for the vulcanization reaction (0-3 wt %). We present an advanced spectroscopic method to chemically analyze the vulcanizing system in rubber under ambient conditions, and we demonstrate a novel application to measure the elements in-line of industrial rubber production. The laser-induced breakdown spectroscopy (LIBS) technique is optimized to ablate material from the surface of produced rubber sheets and to measure the optical emission of S and Zn from the rubber plasma in air. The sulfur lines in the near-infrared range are masked by molecular emission bands of the C-N radical and spectrally interfered by atomic lines of O. Plasma excitation in collinear double-pulse geometry and detection of plasma emission with time-gated detectors suppresses the spectroscopic overlays and enables to resolve the sulfur lines. For the determination of ZnO the weak Zn lines in the ultraviolet range are measured due to their superior intensity stability compared to the much stronger lines in the deeper UV. S and ZnO are quantified in three different rubber materials prepared from the most important polymers used in rubber production. The mean error of prediction of concentrations RMSEP is ≤0.07 wt % for S and ≤0.33 wt % for ZnO for all polymer types. Our results demonstrate that the vulcanizing system of rubber can be quantified under ambient conditions with LIBS. Other chemical elements could be analyzed also and the rubber production could be controlled employing this multielement detection technique as process analytical sensor.
RESUMEN
Laser-induced breakdown spectroscopy (LIBS) for composition analysis of polymer materials results in optical spectra containing atomic and ionic emission lines as well as molecular emission bands. In the present work, the molecular bands are analyzed to obtain spectroscopic information about the plasma state in an effort to quantify the content of different elements in the polymers. Polyethylene (PE) and a rubber material from tire production are investigated employing 157nmF2 laser and 532nm Nd:YAG laser ablation in nitrogen and argon gas background or in air. The optical detection reaches from ultraviolet (UV) over the visible (VIS) to the near infrared (NIR) spectral range. In the UV/VIS range, intense molecular emissions, C2 Swan and CN violet bands, are measured with an Echelle spectrometer equipped with an intensified CCD camera. The measured molecular emission spectra can be fitted by vibrational-rotational transitions by open access programs and data sets with good agreement between measured and fitted spectra. The fits allow determining vibrational-rotational temperatures. A comparison to electronic temperatures Te derived earlier from atomic carbon vacuum-UV (VUV) emission lines show differences, which can be related to different locations of the atomic and molecular species in the expanding plasma plume. In the NIR spectral region, we also observe the CN red bands with a conventional CDD Czerny Turner spectrometer. The emission of the three strong atomic sulfur lines between 920 and 925nm is overlapped by these bands. Fitting of the CN red bands allows a separation of both spectral contributions. This makes a quantitative evaluation of sulfur contents in the start material in the order of 1wt% feasible.