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1.
Soran Shwan Louise Olsson Magnus Skoglundh Jonas Jansson 《American Institute of Chemical Engineers》2015,61(1):215-223
The focus of this work is to investigate whether a previously developed microkinetic deactivation model for hydrothermally treated Fe‐BEA as NH3‐SCR catalyst can be applied to describe chemical deactivation of Fe‐BEA due to phosphorous exposure. The model describes the experiments well for Fe‐BEA before and after phosphorous exposure by decreasing the site density, representing deactivation of sites due to formation of metaphosphates blocking the active iron sites, while the kinetic parameters are kept constant. Furthermore, the results show that the activity for low‐temperature selective catalytic reduction (SCR) is very sensitive to loss of active monomeric iron species due to phosphorous poisoning compared to high‐temperature SCR. Finally, the ammonia inhibition simulations show that exposure to phosphorous may affect the internal transport of ammonia between ammonia storage sites buffering the active iron sites, which results in a lower SCR performance during transient conditions. © 2014 American Institute of Chemical Engineers AIChE J, 61: 215–223, 2015 相似文献
2.
Özlem Erol Till F. Schäberle Dr. Alexander Schmitz Shwan Rachid Dr. Cristian Gurgui Dr. Mustafa El Omari Friederike Lohr Stefan Kehraus Dr. Jörn Piel Prof. Dr. Rolf Müller Prof. Dr. Gabriele M. König Prof. Dr. 《Chembiochem : a European journal of chemical biology》2010,11(9):1253-1265
Corallopyronin A is a myxobacterial compound with potent antibacterial activity. Feeding experiments with labelled precursors resulted in the deduction of all biosynthetic building blocks for corallopyronin A and revealed an unusual feature of this metabolite: its biosynthesis from two chains, one solely PKS‐derived and the other NRPS/PKS‐derived. The starter molecule is believed to be carbonic acid or its monomethyl ester. The putative corallopyronin A biosynthetic gene cluster is a trans‐AT‐type mixed PKS/NRPS gene cluster, containing a β‐branching cassette. Striking features of this gene cluster are a NRPS‐like adenylation domain that is part of a PKS‐type module and is believed to be responsible for glycine incorporation, as well as split modules with individual domains occurring on different genes. It is suggested that CorB is a trans‐acting ketosynthase and it is proposed that it catalyses the Claisen condensation responsible for the interconnection of the two chains. Additionally, the stereochemistry of corallopyronin A was deduced by a combination of a modified Mosher's method and ozonolysis with subsequent chiral GC analyses. 相似文献
3.
O. Pana R. Turcu M.L. Soran C. Leostean E. Gautron C. Payen O. Chauvet 《Synthetic Metals》2010,160(15-16):1692-1698
In this work we report the synthesis and characterization of the nanomagnetic perovskite Sr manganites covered with Au shells having different thickness. La2/3Sr1/3MnO3 (LSMO) manganite nanoparticles were first prepared by a sol–gel procedure. The LSMO manganite nanoparticles were chemically covered with gold to produce the core–shell samples. TEM, HRTEM and atomic emission spectroscopy techniques were used to determine the morphology and structure of the LSMO@Au nanoparticles. The bare LSMO nanoparticles have a mean diameter of around 4.4 nm while LSMO@Au nanoparticles have mean diameters between 7.15 and 4.8 nm depending on the gold quantity involved in the capping process. XRD studies show that both core and shell systems have the expected crystalline structure. The formation of the core–shell structure is sustained by the shift of the plasmon resonance wavelength maximum observed in the UV–vis absorbtion spectra of the LSMO@Au samples depending on the gold concentration. The magnetization versus applied magnetic field of the bare LSMO nanoparticles and LSMO@Au samples shows no hysteresis loop indicating the superparamagnetic behavior of these systems. The analysis of the temperature dependences of FC and ZFC magnetizations shows that for all the samples the axial anisotropy energy barriers are increased due to the magnetic dipolar interactions between neighbor nanoparticles. 相似文献
4.
Liquid–Liquid Diffusion‐Assisted Crystallization: A Fast and Versatile Approach Toward High Quality Mixed Quantum Dot‐Salt Crystals
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Marcus Adam Zhiyu Wang Aliaksei Dubavik Gordon M. Stachowski Christian Meerbach Zeliha Soran‐Erdem Christin Rengers Hilmi Volkan Demir Nikolai Gaponik Alexander Eychmüller 《Advanced functional materials》2015,25(18):2638-2645
Here, a new, fast, and versatile method for the incorporation of colloidal quantum dots (QDs) into ionic matrices enabled by liquid–liquid diffusion is demonstrated. QDs bear a huge potential for numerous applications thanks to their unique chemical and physical properties. However, stability and processability are essential for their successful use in these applications. Incorporating QDs into a tight and chemically robust ionic matrix is one possible approach to increase both their stability and processability. With the proposed liquid–liquid diffusion‐assisted crystallization (LLDC), substantially accelerated ionic crystallization of the QDs is shown, reducing the crystallization time needed by one order of magnitude. This fast process allows to incorporate even the less stable colloids including initially oil‐based ligand‐exchanged QDs into salt matrices. Furthermore, in a modified two‐step approach, the seed‐mediated LLDC provides the ability to incorporate oil‐based QDs directly into ionic matrices without a prior phase transfer. Finally, making use of their processability, a proof‐of‐concept white light emitting diode with LLDC‐based mixed QD‐salt films as an excellent color‐conversion layer is demonstrated. These findings suggest that the LLDC offers a robust, adaptable, and rapid technique for obtaining high quality QD‐salts. 相似文献
5.
Semiconductor Nanocrystals: Liquid–Liquid Diffusion‐Assisted Crystallization: A Fast and Versatile Approach Toward High Quality Mixed Quantum Dot‐Salt Crystals (Adv. Funct. Mater. 18/2015)
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6.
Sialic acid (Sia) is considered as one of the most important biomolecules of life since its derivatives and terminal orientations on cell membranes and macromolecules play a major role in many biological and pathological processes. To date, there is only a limited number of active molecules that can selectively bind to Sia and this limitation has made the study of this glycan challenging. The lectin superfamily is a well-known family of glycan binding proteins, which encompasses many strong glycan binding peptides with diverse glycan affinities. Mistletoe lectin (ML) is considered one of the most active members of lectin family which was initially classified in early studies as a galactose binding lectin; more recent studies have suggested that the peptide can also actively bind to Sia. However, the details with respect to Sia binding of ML and the domain responsible for this binding are left unanswered because no comprehensive studies have been instigated. In this study, we sought to identify the binding domain responsible for the sialic acid affinity of mistletoe lectin isoform I (MLI) in comparison to the binding activity of elderberry lectin isoform I (SNA), which has long been identified as a potent Sia binding lectin. In order to execute this, we performed computational carbohydrate-protein docking for MLB and SNA with Neu5Ac and β-Galactose. We further analyzed the coding sequence of both lectins and identified their glycan binding domains, which were later cloned upstream and downstream to green fluorescent protein (GFP) and expressed in Escherichia coli (E. coli). Finally, the glycan affinity of the expressed fusion proteins was assessed by using different biochemical and cell-based assays and the Sia binding domains were identified. 相似文献
7.
Rachid S Huo L Herrmann J Stadler M Köpcke B Bitzer J Müller R 《Chembiochem : a European journal of chemical biology》2011,12(6):922-931
The cinnabaramides and salinosporamides are mixed PKS/NRPS natural products isolated from a terrestrial streptomycete and a marine actinomycete, respectively. They interfere with the proteasome and thus potentially inhibit the growth of cancer cells. The compounds exhibit a γ-lactam-β-lactone bicyclic ring structure attached to a cyclohexenyl unit and a PKS side chain. As a first step towards improving anticancer activity and permitting genetic approaches to novel analogues, we have cloned and characterized the cinnabaramide biosynthetic genes from Streptomyces sp. JS360. In addition to the expected PKS and NRPS genes, the cluster encodes functionalities for the assembly of the hexyl side chain precursor. The corresponding enzymes exhibit relaxed substrate specificities towards a number of synthesized precursors, enabling production of novel chlorinated cinnabaramides. These were isolated and analyzed for activity, revealing that derivatives bearing a chlorine atom in the PKS side chain show higher inhibitory potentials towards the proteasome's proteolytic subunits (especially the trypsin and chymotrypsin units) and higher cytotoxicities towards human tumor cell lines than the parent cinnabaramide A. Although their activities towards the proteasome were weaker than that of salinosporamide A, the cinnabaramides were found to inhibit the growth of various fungi with greater potency. 相似文献
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9.
Sahar Moharrerzadeh Kurd Soran Hassanifard Stefan Hartmann 《Iranian Polymer Journal》2017,26(4):253-260
The aim of this work is to investigate the fracture characteristics of the epoxy-based stepped functionally graded materials (FGM) reinforced with carbon nanotubes (CNTs). The effects regarding fracture toughness in mode I were also studied. The specimens were fabricated with three different mass percentages of 0.1, 0.2 and 0.3%. An ultrasonic device was used to disperse the carbon nanotubes to have a uniform mixture without agglomeration of the CNT particles. Using the ASTM standard D-5045, the fracture toughness was obtained in the experiments. Some compact tension specimens were tested in a tensile machine in mode I. Two different notches were investigated to calculate the fracture toughness. For each notch, there were different fracture toughness and fracture forces values. The experiments showed that there is an improvement in the fracture resistance of FGMs and non-graded composite materials by increase in the CNTs content. The materials with the same content of carbon nanotubes do not have the same properties. It is seen that high fracture toughness can be obtained from different CNT content materials in each notch. In fact, the size of the notch affects the results. Comparing the fracture toughness values and fracture forces results showed that there is no specified rule to predict the increase in the fracture characteristics by increasing carbon nanotubes content. Fracture characteristics depend on the important parameters such as the size of the notch, CNTs content and dispersion of the carbon nanotubes. 相似文献
10.
Soran Hassanifard Mohammad Zehsaz Firooz Esmaeili 《Journal of Mechanical Science and Technology》2011,25(3):647-653
In the present study, the effects of spot weld arrangements in multi-spot welded joints on the fatigue behavior of the joints
are studied. Three different four-spot welded joints are considered: one-row four-spot parallel to the loading direction,
one-row four-spot perpendicular to the loading direction and two-row four-spot weld specimens. The experimental fatigue test
results reveal that the differences between the fatigue lives of three spot welded types in the low cycle regime are more
considerable than those in the high cycle regime. However, all kinds of spot weld specimens have similar fatigue strength
when approaching a million cycles. A non-linear finite element analysis is performed to obtain the relative stress gradients,
effective distances and notch strength reduction factors based on the volumetric approach. The work here shows that the volumetric
approach does a very good job in predicting the fatigue life of the multi-spot welded joints. 相似文献