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71.
72.
Die Bestimmung des Grenzumformgrades eines Stahles, der während der plastischen Verformung nicht überschritten werden kann, ist von großer Bedeutung. Die vorliegende Arbeit berichtet über Ergebnisse von Warmtorsionsversuchen, aus denen der Grenzumformgrad als Funktion von Temperatur und Umformgeschwindigkeit ermittelt wurde. Die Versuche wurden an den Stählen X 10 CrNiTi 18 9, 10 CrMo 9 10, X 10 CrNiMoTi 18 12, X 20 CrMoV 12 1 und X 2 NiCrNb 25 18 durchgeführt. 相似文献
73.
74.
Most of the bountiful literature on the calculation of effectiveness factors for catalyst particles deals with relatively simple reactions and kinetics. The performance of catalyst particles in the industrially important, modified Claus reaction introduces multiple reactions, sulphur vapour equilibria, non-linear kinetics and limiting thermodynamic conversions into the calculation of local effectiveness factors. This analysis demonstrates a means for generating local effectiveness factors, during reactor design calculations by the use of a single calculated curve of versus a modified Thiele parameter for spherical particles. 相似文献
75.
Ivo Allegrini Claudio Battistoni Giulia Mattogno Ernesto Paparazzo 《The Science of the total environment》1981,19(3):223-232
The capability of X-ray photoelectron spectroscopy, XPS or ESCA, in analysing oxidation states and measuring the concentration of elements present in air pollution particulates collected on membrane filters is evaluated. Semi-quantitative data are compared with those from XRF and wet chemical analysis. Differences of about a factor of 2.0–2.5 are found which are critically discussed in relation to particle size and the distribution of ionic species. The importance of intrinsic properties of matrix materials and instrumental factors is also discussed. 相似文献
76.
Staggemeier BA Bramanti E Allegrini C Skogerboe KJ Synovec RE 《Analytical chemistry》2005,77(1):250-258
Using flow injection analysis (FIA), a pH gradient is blended in real time with a protein sample as the pH-dependent protein surface activity is measured by a dynamic surface tension detector (FIA-pH-DSTD). This instrumental system was developed as a high-throughput method for the screening of protein surface activity at the air/liquid interface as a function of pH. This method utilizes the continuous flow, drop-based dynamic surface tension detector in combination with flow injection sample introduction and blending of a steady-state concentration of protein sample with a pH gradient ranging from pH 2.0 to pH 11.5. Dynamic surface tension is measured through the differential pressure across the air/liquid interface of repeatedly growing and detaching drops. Continuous surface tension measurement is achieved for each eluting drop of 2-s length (2 muL), providing insight into both the kinetic and thermodynamic behaviors of molecular orientation processes at the liquid/air interface. Three-dimensional data are obtained, with surface tension first converted to surface pressure, which is collected as a function of elution time versus drop time. In FIA-pH-DSTD, a commercial pH probe is used to measure pH during elution time, enabling surface pressure throughout drop time to be subsequently plotted as a function of eluting pH. An automated DSTD calibration procedure and data analysis method is applied, which allows simultaneous use of two different solvents, permitting real-time dynamic surface tension data to be obtained. The method was applied to the analysis of 14 commercial purified proteins, yielding characteristic features of surface activity as a function of pH. The reproducibility of the measurement and selectivity advantage of the DSTD was shown for the analysis of serum albumins from various mammalian sources. Several applications were also suggested and discussed in order to show the potential of the method for protein and food chemistry studies and in the study of protein-polymer interactions. 相似文献
77.
78.
Leona Buňková František Buňka Gabriela Mantlová Andrea Čablová Ivo Sedláček Pavel Švec Vendula Pachlová Stanislav Kráčmar 《Food microbiology》2010
The aim of the work was to describe the development of selected biogenic amines (histamine, tyramine, putrescine and cadaverine) in 4 layers of Dutch-type cheese (Edam-cheese) depending on 3 ripening/storage regimes during a 98-day period. Biogenic amines were analysed by means of ion-exchange chromatography. A further goal was to identify microbial sources of biogenic amines in the material analysed. Phenotype characterization and repetitive sequence-based PCR fingerprinting were used to identify the isolated bacteria. The highest content of tyramine, putrescine and cadaverine was determined in cheeses stored in a ripening cellar at a temperature of 10 °C during the whole observation period. Lower biogenic amines content was determined in samples which were moved into a cold storage device (5 °C) after 38 days of storage in a ripening cellar (10 °C). The lowest concentrations of biogenic amines were detected in cheeses which were moved into a cold storage device (5 °C) after 23 days of storage in a ripening cellar (10 °C). During the 98-day period, histamine was not detected in any of the regimes. Within the cheeses analysed, non-starter lactic acid bacteria Lactobacillus curvatus, Lactobacillus casei/paracasei and Lactobacillus plantarum were detected as the main producers of the biogenic amines tested. In starter bacteria Lactococcus lactis subsp. lactis and Lactococcus lactis subsp. cremoris the decarboxylase activity tested was not detected. 相似文献
79.
Altelaar AF Klinkert I Jalink K de Lange RP Adan RA Heeren RM Piersma SR 《Analytical chemistry》2006,78(3):734-742
Surface metallization by plasma coating enhances desorption/ionization of membrane components such as lipids and sterols in imaging time-of-flight secondary ion mass spectrometry (TOF-SIMS) of tissues and cells. High-resolution images of cholesterol and other membrane components were obtained for neuroblastoma cells and revealed subcellular details (resolving power 1.5 mum). Alternatively, in matrix-enhanced SIMS, 2,5-dihydroxybenzoic acid electrosprayed on neuroblastoma cells allowed intact molecular ion imaging of phosphatidylcholine and sphingomyelin at the cellular level. Gold deposition on top of matrix-coated rat brain tissue sections strongly enhanced image quality and signal intensity in stigmatic matrix-assisted laser desorption/ionization imaging mass spectrometry. High-quality total ion count images were acquired, and the neuropeptide vasopressin was localized in the rat brain tissue section at the hypothalamic area around the third ventricle. Although the mechanism of signal enhancement by gold deposition is under debate, the results we have obtained for cells and tissue sections illustrate the potential of this sample preparation technique for biomolecular surface imaging by mass spectrometry. 相似文献
80.
This work identifies electrical field-induced concentration polarization (CP) as a key physical mechanism influencing the retention behavior of charged analytes in electrochromatography with fixed beds of porous adsorbent particles. Due to an insufficient screening of intraparticle surface charge, under most general conditions the porous (permeable) particles become charge-selective. CP is caused by coupled mass and charge transport normal to the charge-selective external surface of the permeable particles, which leads to concentration gradients of ionic species in the adjoining interparticle electrolyte solution. Cation-exchange (cation-selective) particles were employed to investigate the influence of applied voltage on the retention factor of counterionic, i.e., positively charged, analytes. It is demonstrated by macroscopic retention data and microscopic studies resolving the CP phenomenon on a particle scale that the dependence of CP on electrical field and mobile-phase ionic strengths is directly reflected in concomitant changes of analyte retention. The CP zones that develop at the interface between interparticle and intraparticle pore space are recognized by charged, but not electroneutral analytes while entering or leaving the particles. The intensity of these convective-diffusion boundary layers (CP zones) depends on the applied field strength and charge selectivity of a particle. Thus, it is the charge-selective transport between the interparticle and intraparticle pore space in packed beds that prevails under typical experimental conditions in electrochromatography and that forms the physical basis for a general electrical field dependence of the retention factor of charged analytes. 相似文献