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Organisationseinheit der BAM
One of the most commonly used bonds between two biomolecules is the bond between biotin and streptavidin (SA) or streptavidin homologues (SAHs). A high dissociation constant and the consequent high-temperature stability even allows for its use in nucleic acid detection under polymerase chain reaction (PCR) conditions. There are a number of SAHs available, and for assay design, it is of great interest to determine as to which SAH will perform the best under assay conditions. Although there are numerous single studies on the characterization of SAHs in solution or selected solid phases, there is no systematic study comparing different SAHs for biomolecule-binding, hybridization, and PCR assays on solid phases. We compared streptavidin, core streptavidin, traptavidin, core traptavidin, neutravidin, and monomeric streptavidin on the surface of microbeads (10–15 μm in diameter) and designed multiplex microbead-based experiments and analyzed simultaneously the binding of biotinylated oligonucleotides and the hybridization of oligonucleotides to complementary capture probes. We also bound comparably large DNA origamis to capture probes on the microbead surface. We used a real-time fluorescence microscopy imaging platform, with which it is possible to subject samples to a programmable time and temperature profile and to record binding processes on the microbead surface depending on the time and temperature. With the exception of core traptavidin and monomeric streptavidin, all other SA/SAHs were suitable for our investigations. We found hybridization efficiencies close to 100% for streptavidin, core streptavidin, traptavidin, and neutravidin. These could all be considered equally suitable for hybridization, PCR applications, and melting point analysis. The SA/SAH–biotin bond was temperature-sensitive when the oligonucleotide was mono-biotinylated, with traptavidin being the most stable followed by streptavidin and neutravidin. Mono-biotinylated oligonucleotides can be used in experiments with temperatures up to 70 °C. When oligonucleotides were bis-biotinylated, all SA/SAH–biotin bonds had similar temperature stability under PCR conditions, even if they comprised a streptavidin variant with slower biotin dissociation and increased mechanostability.
During R/V Meteor cruise 141/1, pore fluids of near surface sediments were investigated to find indications for hydrothermal activity in the Terceira Rift (TR), a hyperslow spreading center in the Central North Atlantic Ocean. To date, submarine hydrothermal fluid venting in the TR has only been reported for the D. João de Castro seamount, which presently seems to be inactive. Pore fluids sampled close to a volcanic cone at 2,800‐m water depth show an anomalous composition with Mg, SO4, and total alkalinity concentrations significantly higher than seawater and a nearby reference core. The most straightforward way of interpreting these deviations is the dissolution of the hydrothermally formed mineral caminite (MgSO4 0.25 Mg (OH)2 0.2H2O). This interpretation is corroborated by a thorough investigation of fluid isotope systems (δ26Mg, δ30Si, δ34S, δ44/42Ca, and 87Sr/86Sr). Caminite is known from mineral assemblages with anhydrite and forms in hydrothermal recharge zones only under specific conditions such as high fluid temperatures and in altered oceanic crust, which are conditions generally met at the TR. We hypothesize that caminite was formed during hydrothermal activity and is now dissolving during the waning state of the hydrothermal system, so that caminite mineralization is shifted out of its stability zone. Ongoing fluid circulation through the basement is transporting the geochemical signal via slow advection toward the seafloor.
In the literature there are not much data available to describe the corrosion behavior of titanium, nickel alloys and special stainless steels in acids at high temperature, in particular above the boiling point. Therefore, a laboratory testing program was performed with two titanium alloys (grade 2 - UNS R50400 and grade 12 - UNS R53400) to obtain corrosion data in formic acid, acetic acid, phosphoric acid, polyphosphoric acid, p-toluene sulfonic acid and lactic acid at 200 °C. Results were compared to previously published ones obtained on alloy 31 (UNS N08031), alloy 59 (UNS N06059) and B-2 (UNS N10665).
From the results it can be concluded that titanium does not always Show better corrosion resistance than Ni-based alloys,
Alloy 59 was the best choice for formic and acetic acids at temperatures of 200°C. Both Ti-alloys are resistant in acetic acid. Some slight differences were observed for formic acid, where Ti grade 2 is only resistant up to a 20 % solution and grade 12 in concentrated acid too. The phosphoric acid is extremely corrosive and none of the investigated materials was resistant. In the diluted acid (5 %) only Ti grade 12 is resistant, whereas in 1 % solution all investigated materials withstand. Alloy B-2 and alloy 59 showed the best behavior in polyphosphoric acid. In 30 % concentrated p-toluene sulfonic acid at 200 °C all alloys tested were unsuitable. In very diluted acid (0.1 %) both Ti-alloys and the other three alloys behaved well. In lactic acid at 180 °C increased corrosion underneath deposits was detected; the best performance was observed for alloy 59 and Ti grade 2.
In the literature there are not much data available to describe the corrosion behavior of titanium, nickel alloys and special stainless steels in acids at high temperature, in particular above the boiling point. Therefore, a laboratory testing program was performed with two titanium alloys (UNS R50400 and UNS R53400) to obtain corrosion data in formic acid, acetic acid, phosphoric acid, polyphosphoric acid, p-toluene sulfonic acid and lactic acid at 200 °C. Results were compared to previously published ones obtained on UNS N08031, UNS N06059 and UNS N10665.
From the results it can be concluded that titanium does not always show better corrosion resistance than Ni-based alloys.
UNS N06059 was the best choice for formic and acetic acids at temperatures of 200 °C. Both Ti-alloys are resistant in acetic acid. Some slight differences were observed for formic acid, where UNS R50400 is only resistant up to a 20 % solution and UNS R53400 in concentrated acid too. The phosphoric acid is extremely corrosive and none of the investigated materials was resistant. In the diluted acid (5 %) only UNS R53400 is resistant, whereas in 1 % solution all investigated materials performed satisfactory. UNS N10665 and UNS N06059 showed the best behavior in polyphosphoric acid. In 30 % concentrated p-toluene sulfonic acid at 200 °C all alloys tested were unsuitable. In very diluted acid (0.1 %) both Ti-alloys and the other three alloys behaved well. In lactic acid at 180 °C increased corrosion underneath deposits was detected; the best performance was observed for UNS N06059 and UNS R50400.
Microbead-based technologies represent elegant and versatile approaches for highly parallelized quantitative multiparameter assays. They also form the basis of various techniques for detection and quantification of nucleic acids and proteins. Nucleic acid-based methods include hybridization assays, solid-phase PCR, sequencing, and trapping assays. Microbead assays have been improved in the past decades and are now important tools in routine and point-of-care diagnostics as well as in life science. Its advances include low costs, low workload, high speed and high-throughput automation. The potential of microbead-based assays therefore is apparent, and commercial applications can be found in the detection and discrimination of single nucleotide polymorphism, of pathogens, and in trapping assays. This review provides an overview on microbead-based platforms for biosensing with a main focus on nucleic acid detection (including amplification strategies and on selected probe systems using fluorescent labeling). Specific sections cover chemical properties of microbeads, the coupling of targets onto solid surfaces, microbead probe systems (mainly oligonucleotide probes), microbead detection schemes (with subsections on suspension arrays, microfluidic devices, and immobilized microbeads), quantification of nucleic acids, PCR in solution and the detection of amplicons, and methods for solid-phase amplification. We discuss selected trends such as microbead-coupled amplification, heterogeneous and homogenous DNA hybridization assays, real-time assays, melting curve analysis, and digital microbead assays. We finally discuss the relevance and trends of the methods in terms of high-level multiplexed analysis and their potential in diagnosis and personalized medicine. Contains 211 references.
Fe-ZSM-5 Catalysts for the Selective Reduction of NO by Isobutane - The Problem of the Active Sites
(2002)
Relations between the structure of FeZSM-5 catalysts prepared by interaction of FeCl3 with HZSM-5 and their catalytic behavior in the SCR of NO by isobutane were investigated by combining results of catalytic studies (1000 ppm NO, 1000 ppm isobutane, and 2% O2 in He, 30,000 h-1) and of physicochemical characterization (XRD, EXAFS, Mössbauer spectroscopy, TPR, IR, XPS). By variation of the preparation conditions (method of FeCl3 introductionchemical vapor deposition or solid-state ion exchange, washing intensity, calcination regime) and of the matrix (HZSM-5 with normal and high defect density), FeZSM-5 materials with strongly varying properties (aggregation degree of the Fe phase, acidity) were obtained. Significant discrepancies between conclusions derived from EXAFS, TPR, and Mössbauer spectroscopy were ascribed to a preference of Mössbauer spectroscopy for the detection of aggregated phases and a high defectivity of Fe oxide clusters formed upon calcination. The critical step for the preparation of a highly disperse Fe phase is extensive washing after Fe introduction. The catalytic behavior of overexchanged FeZSM-5 materials prepared by interaction of FeCl3 with HZSM-5 of normal defect density was not influenced by aggregation of a significant part of the Fe phase. The comparison of their catalytic properties with those of a Fe2O3/HZSM-5 mechanical mixture and of catalysts prepared by aqueous ion exchange or by CVD of FeCl3 into HZSM-5 of high defect density implies that the particular activity of overexchanged FeZSM-5 arises from minority sites. In these, the Fe ions are probably isolated. Other Fe sites of low nuclearity appear to add to the activity. The poor SCR performance (at a given ability for isobutane activation) of FeZSM-5 prepared with a defective ZSM-5 matrix may indicate that the Fe sites which provi de the particular activity of overexchanged FeZSM-5 require the cooperation of acidic sites.