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Werner Heimann Karl-Heinz Franzen Adolf Rappe und Herbert Ullemeyer 《Zeitschrift für Lebensmitteluntersuchung und -Forschung A》1976,162(2):109-114
Zusammenfassung Während der Incubation von Soja-Lipoxygenase mit Linolsäure entstehen flüchtige Verbindungen, für deren Genese sich mindestens zwei Möglichkeiten abzeichnen: Die eine Möglichkeit besteht darin, daß aus bereits vorgebildeten Linolsäurehydroperoxiden Spaltprodukte auftreten. Zum andern können — je nach äußeren Bedingungen (Temperatur, O2-Druck, Partnerkonzentration, u.a.) — flüchtige Stoffe verschiedener chemischer Natur aus radikalischen Reaktionszwischenstufen entstehen. Durch Versuche mit Hydroperoxid-abbauenden Enzymen (Peroxidasen) und unter Verwendung radioaktiv markierter Linolsäurehydroperoxide wurden die angedeuteten Bildungswege untersucht. Unsere epxerimentellen Ergebnisse zeigen, daß die Bildung der hier untersuchten flüchtigen Verbindungen aus Reaktionszwischenstufen vor sich geht. Festzuhalten ist jedoch, daß n-Hexanal neben der Bildung aus Reaktionszwischenstufen auch aus dem Zerfall vorher gebildeter Hydroperoxide entsteht. Das schon von uns früher angegebene Rekationsschema [2] konnte nunmehr durch diese Untersuchungen experimentell gesichert werden.
Herrn Prof. Dr. J. Eisenbrand zum 75. Geburtstag gewidmet. 相似文献
Investigations on the development of volatile substances during lipoxygenase-linolic-acid-reaction
Summary During incubation of soja-Lipoxygenase with Linolic acid, volatile compounds are formed the development of which can be seen in two possible ways: from preformed Linolic-acid-hydroperoxides splitproducts arise or volatile substances of different chemical nature are built depending on the reaction conditions like temperature, O2-pressure, partner-concentration etc. By trials with hydroperoxdde-decomposing enzymes (peroxidase) and by means of radioactive labelled Linolic-acid-hydroperoxides the pathways mentioned above were investigated. The results indicate that the volatile compounds are built from by-products; n-hexanal was formed from these by-products as well as from decomposed hydroperoxide. The previously proposed reaction-scheme has this been ascertained by experimental means.
Herrn Prof. Dr. J. Eisenbrand zum 75. Geburtstag gewidmet. 相似文献
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B Strandberg L Strandberg B van Bavel PA Bergqvist D Broman J Falandysz C N?f O Papakosta C Rolff C Rappe 《Canadian Metallurgical Quarterly》1998,215(1-2):69-83
Naive T lymphocytes specific for a given primary antigen occur in low frequencies and require the relevant antigen to be presented by specialist antigen presenting cells (APC), i.e., dendritic cells (DC). For these reasons, the in vitro induction of primary T lymphocyte responses remains a significant technical challenge. We have attempted to improve current strategies for generating in vitro responses by optimising (i) isolation and concomitant activation of DC from peripheral blood, (ii) uptake, processing and presentation of antigen by DC and (iii) antigen driven T lymphocyte proliferation. We established that RPMI 1640 media supplemented with 10% autologous serum resulted in the best yield of CMRF-44+, CD14-, CD19- DC after enrichment over a Nycodenz gradient. Optimal presentation of whole protein and peptide antigen was achieved by addition after the purification of the APC, i.e., at the start of the T lymphocyte proliferation assay. RPMI 1640 supplemented with 10% autologous serum or plasma supported the best antigen driven specific T lymphocyte responses. Using these optimised conditions, we compared the efficacy of PBMC and purified blood DC for priming T lymphocyte responses to the chronic myeloid leukaemia (CML) specific bcr-abl (b3a2) peptide. Peptide specific T lymphocyte responses were generated with both purified DC and whole PBMC, suggesting that T lymphocyte precursor frequency was the limiting factor in these experiments. These results will aid in the generation of human T lymphocyte lines to primary antigens, for in vitro and therapeutic applications. 相似文献
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S. H. Shah P. D. Bristowe A. M. Kolpak A. M. Rappe 《Journal of Materials Science》2008,43(11):3750-3760
The geometrical, chemical and ferroelectric properties of a new nanoscale short-period three-component SrTiO3/BaTiO3/PbTiO3 perovskite superlattice are investigated using a first principles density functional approach. The study focuses on varying
the thickness of each component in the superlattice and determining the resulting lattice distortion and total polarization.
Thicknesses of up to three unit cells in a single component are considered and the in-plane lattice constants normal to the
[001] stacking direction are fixed to the bulk SrTiO3 values to simulate a rigid substrate. It is found that the PbTiO3 layers play a key role in strain and polarization enhancement. By increasing the amount of PbTiO3 in the superlattices the strain in the other components increases significantly resulting in an enhanced total polarization
of the superlattice relative to bulk BaTiO3. Increasing the number of BaTiO3 layers also improves the overall polarization. All the SrTiO3 layers in each superlattice are found to be highly polarized. Many of the calculated features are similar to those found
previously by others for the SrTiO3/BaTiO3/CaTiO3 superlattice, although in the present study significantly greater enhancement factors and polarization values are found.
The predicted enhancement of the polarization is mostly attributed to lattice strain due to mismatch of the in-plane lattice
constant of the three-component materials. 相似文献
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Mixed Valence Perovskite Cs2Au2I6: A Potential Material for Thin‐Film Pb‐Free Photovoltaic Cells with Ultrahigh Efficiency
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Lamjed Debbichi Songju Lee Hyunyoung Cho Andrew M. Rappe Ki‐Ha Hong Min Seok Jang Hyungjun Kim 《Advanced materials (Deerfield Beach, Fla.)》2018,30(12)
New light is shed on the previously known perovskite material, Cs2Au2I6, as a potential active material for high‐efficiency thin‐film Pb‐free photovoltaic cells. First‐principles calculations demonstrate that Cs2Au2I6 has an optimal band gap that is close to the Shockley–Queisser value. The band gap size is governed by intermediate band formation. Charge disproportionation on Au makes Cs2Au2I6 a double‐perovskite material, although it is stoichiometrically a single perovskite. In contrast to most previously discussed double perovskites, Cs2Au2I6 has a direct‐band‐gap feature, and optical simulation predicts that a very thin layer of active material is sufficient to achieve a high photoconversion efficiency using a polycrystalline film layer. The already confirmed synthesizability of this material, coupled with the state‐of‐the‐art multiscale simulations connecting from the material to the device, strongly suggests that Cs2Au2I6 will serve as the active material in highly efficient, nontoxic, and thin‐film perovskite solar cells in the very near future. 相似文献
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Modified four-point bending specimen for determining the interface fracture energy for thin, brittle layers 总被引:3,自引:0,他引:3
Ines Hofinger Matthias Oechsner Hans-Achim Bahr Michael V. Swain 《International Journal of Fracture》1998,92(3):213-220
A well-known four-point bending test has been modified such that the critical energy release rate
for delaminating cracks propagating at the interface of a thin, brittle layer bonded to a substrate can be measured. The
energy release rate
required for crack delaminating at those interfaces is obtained by attaching a stiffening layer to the layer system. Another
advantage of this modification is that segmentation of the layer and plastic deformation of the substrate during bending are
avoided. The interface fracture energy
of a plasma sprayed ZrO2-ceramic layer on a flame sprayed high alloyed steel substrate has been measured.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
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Holzhauser C Wagenknecht HA 《Chembiochem : a European journal of chemical biology》2012,13(8):1136-1138
Add it and see it: The concept of "DNA traffic lights" for wavelength-shifting DNA probes has a great potential in the application of biosensors, for example, in DNA aptamers. A visual color change in the DNA aptasensor fluorescence from green to red occurs after specific target binding. 相似文献