43 research outputs found
AVOIDING HARD DECISIONS IN ADAPTIVE WATERMARKING
ABSTRACT In this paper, we describe the coupling of content adaptive watermark decoding and soft-decision forward error correction. We deduce three fundamental properties from adaptive watermarking methods switching between different embedding strengths. It is shown how a weighting process at the decoder can be used to build up an overall soft processing watermarking. No pre-distortion has to be used, and hence, the image quality is not degraded. In this conjunction, even adaptation techniques can be used where it is computational infeasible to project a pre-distortion back onto the host image. Experimental results indicate the improvement in bit error correction during watermark retrieval by a factor of 5. Without loss of security, performance or functionality our new technique can be integrated very easily into numerous watermarking applications
Multi-modal investigation of the bone micro- and ultrastructure, and elemental distribution in the presence of Mg-xGd screws at mid-term healing stages
Magnesium (Mg) – based alloys are becoming attractive materials for medical applications as temporary bone implants for support of fracture healing, e.g. as a suture anchor. Due to their mechanical properties and biocompatibility, they may replace titanium or stainless-steel implants, commonly used in orthopedic field. Nevertheless, patient safety has to be assured by finding a long-term balance between metal degradation, osseointegration, bone ultrastructure adaptation and element distribution in organs. In order to determine the implant behavior and its influence on bone and tissues, we investigated two Mg alloys with gadolinium contents of 5 and 10 wt percent in comparison to permanent materials titanium and polyether ether ketone. The implants were present in rat tibia for 10, 20 and 32 weeks before sacrifice of the animal. Synchrotron radiation-based micro computed tomography enables the distinction of features like residual metal, degradation layer and bone structure. Additionally, X-ray diffraction and X-ray fluorescence yield information on parameters describing the bone ultrastructure and elemental composition at the bone-to-implant interface. Finally, with element specific mass spectrometry, the elements and their accumulation in the main organs and tissues are traced. The results show that Mg-xGd implants degrade in vivo under the formation of a stable degradation layer with bone remodeling similar to that of Ti after 10 weeks. No accumulation of Mg and Gd was observed in selected organs, except for the interfacial bone after 8 months of healing. Thus, we confirm that Mg-5Gd and Mg-10Gd are suitable material choices for bone implants
Modification of tricine–SDS–PAGE for online and offline analysis of phosphoproteins by ICP-MS
Qualitative and Quantitative Evaluation of Sulfur-Containing Compound Types in Heavy Crude Oil and Its Fractions
Detailed molecular analysis of complex mixtures such as crude oil and its fractions has been successfully covered by a number of groups during the past two decades. On the other side, the most glaring need is some type of method that allows quantitative analysis of a single class, compound species, or even individual compounds. Here, the problem is being complicated by the complexity of the sample and the need for individual response factors necessary for the analysis of single compounds in almost all analytical methods. This can be circumvented by using a method with uniform response like inductively coupled plasma-mass spectrometry. Sulfur is one of the most important heteroelements present in crude oil and its products due to stringent regulations. Quantification of sulfur by means of mass spectrometry has always been a challenging task. Here, we present the combination of a sulfur-selective chromatographic separation of crude oil and its fractions on a Pd-coated stationary phase with two-dimensional detection. Qualitative analysis by ultrahigh-resolution Orbitrap mass spectrometry allows a detailed understanding of individual compositions after chromatographic separation, while the quantitative data from inductively coupled plasma tandem mass spectrometry details the quantities of each part of the chromatogram. The combination of the results from both methods allows assigning three different types of sulfur species and their quantitative determination in extremely complex heavy crude oil fractions
C-reactive protein in blood plasma and serum samples of harbor seals (<i>Phoca vitulina</i>)
Quantitative and Qualitative Analysis of Three Classes of Sulfur Compounds in Crude Oil
Owing to the environmental hazards arising from sulfur‐containing combustion products, strong legal regulations exist to reduce the sulfur content of transportation fuels down to a few ppm. With the ongoing depletion of low‐sulfur crude oil reservoirs, increased technological efforts are needed for crude oil refining to meet these requirements. The desulfurization step is a critical part of the refining process but partly suffers from the recalcitrance of certain species to sulfur removal and the inability to quantitatively understand the behavior of individual compound classes during the process. We herein present a new and simple approach for the parallel quantification of three different classes of sulfur species present in crude oils by LC separation and on‐line detection and quantification by ICP‐MS/MS. This approach will help to estimate the amount of recalcitrant species and thus facilitate the optimization of desulfurization conditions during fuel production
