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951.
Dissimilar material joining using laser (aluminum to steel using zinc-based filler wire) 总被引:9,自引:0,他引:9
Alexandre Mathieu Rajashekar Shabadi Alexis Deschamps Michel Suery Simone Matteï Dominique Grevey Eugen Cicala 《Optics & Laser Technology》2007,39(3):652-661
Joining steel with aluminum involving the fusion of one or both materials is possible by laser beam welding technique. This paper describes a method, called laser braze welding, which is a suitable process to realize this structure. The main problem with thermal joining of steel/aluminum assembly with processes such as TIG or MIG is the formation of fragile intermetallic phases, which are detrimental to the mechanical performances of such joints. Braze welding permits a localized fusion of the materials resulting in a limitation on the growth of fragile phases. This article presents the results of a statistical approach for an overlap assembly configuration using a filler wire composed of 85% Zn and 15% Al. Tensile tests carried on these assemblies demonstrate a good performance of the joints. The fracture mechanisms of the joints are analyzed by a detailed characterization of the seams. 相似文献
952.
This paper is a continuation of “Diffusions conditionelles, I.” If (xt, zt) is a two-component diffusion process, it is shown that under appropriate conditions, the process xt (t ? T), given (zs, s ? T) is a nonhomogeneous strong Markov process, whose generator is explicitly found by using the theory of stochastic flows. The filtering equation is reduced to an ordinary partial differential equation. 相似文献
953.
954.
Catherine Verchre Dominique Rousselle Claude Viel 《Magnetic resonance in chemistry : MRC》1978,11(8):395-397
Carbon-13 NMR spectra of some dihydro- and tetrahydro-isoquinolines were studied and applied to the assignments of 13C NMR signals of some 8,13-diazasteroids related to the estrone series. Some deuterated compounds were also examined. All signals could be assigned and an important long-range isotopic effect was observed which seems to be due to an interaction between the C? H(D) bond and the nitrogen lone pairs. 相似文献
955.
Consider a continuous time Markov chain with stationary transition probabilities. A function of the state is observed. A regular conditional probability distribution for the trajectory of the chain, given observations up to time t, is obtained. This distribution also corresponds to a Markov chain, but the conditional chain has nonstationary transition probabilities. In particular, computation of the conditional distribution of the state at time s is discussed. For s > t, we have prediction (extrapolation), while s < t corresponds to smoothing (interpolation). Equations for the conditional state distribution are given on matrix form and as recursive differential equations with varying s or t. These differential equations are closely related to Kolmogorov's forward and backward equations. Markov chains with one observed and one unobserved component are treated as a special case. In an example, the conditional distribution of the change-point is derived for a Poisson process with a changing intensity, given observations of the Poisson process. 相似文献
956.
Engeldinger E Armspach D Matt D Jones PG 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(13):3091-3105
The binding properties of two alpha-cyclodextrins, each containing two C(5)-linked "CH(2)PPh(2)" units, L 1 (A,D-substituted) and L 2 (A,C-substituted), have been investigated. Both ligands readily form transition-metal chelate complexes in which the metal centres are immobilised at the cavity entrance. Although diphosphane L 1 displays a marked tendency to behave only as a trans-spanning ligand, the ligand possesses a certain degree of flexibility, for example, allowing the stabilisation of a trigonal silver(I) complex in which the bite angle drops to 143 degrees. Another feature of L 1 concerns its ability to function as an hemilabile ligand. Together with four methoxy groups anchored onto the primary face, the two P(III) centres of L 1 form a circularly arranged P(2)O(4) 12-electron donor set able to complex an Ag(+) ion in a dynamic way, each of the four oxygen atoms coordinating successively to the silver ion. Furthermore, the particular structures of L 1 and L 2, characterised by the presence of P(III) units lying close to the cavity entrance, lead upon complexation to complexes whereby the first coordination sphere is partly entrapped in the cyclodextrin. Thus, when treated with metal chlorides, both ligands systematically produce complexes in which the Mbond;Cl unit is maintained inside the cyclodextrin through weak Cl.H-5 interactions. The chelate complex [Ag(L 1)]BF(4) reacts with acetonitrile in excess to afford a mixture of two equilibrating complexes, [Ag(acetonitrile)(L 1)]BF(4) and [Ag(acetonitrile)(2)(L 1)]BF(4), whose coordinated nitriles lie inside the cyclodextrin cavity. The inner-cavity ligands can be substituted by a benzonitrile molecule. The present study provides the first identification of an [Ag(acetonitrile)(2)(phosphane)(2)](+) ion. The unexpected stabilisation of this species probably rests on a cavity effect, the cyclodextrin walls favouring recombination of the complex after facile dissociation of the nitrile ligands. 相似文献
957.
Bonnet D Grandjean C Rousselot-Pailley P Joly P Bourel-Bonnet L Santraine V Gras-Masse H Melnyk O 《The Journal of organic chemistry》2003,68(18):7033-7040
A novel procedure for the preparation of alpha-hydrazinoacetyl peptides is reported on the basis of the solid-phase coupling of partially or fully Boc-protected hydrazino acetic acid derivatives. The degree of unwanted polymerization of the activated ester during both activation and coupling was found to be significant for the monoprotected derivative BocNHNHCH(2)CO(2)H but could be minimized with the diprotected derivative BocNHNH(Boc)CH(2)CO(2)H and suppressed with the fully protected acid. Despite the instability of the imidocarbonate group toward acids and bases, a low-cost and effective route was sought for the preparation of the tris(Boc)-protected derivative. The N,N,N'-tris(Boc)hydrazinoacetic acid could be introduced on the solid phase after or before peptide elongation using Fmoc/tert-butyl chemistry. In this latter case, HR MAS NMR analysis of model solid supports demonstrated the partial loss of one Boc group during the repetitive piperidine treatments. Despite this slight instability, N,N,N'-tris(Boc)hydrazinoacetic acid was found to be a highly convenient reagent for the robust and easily scalable preparation of hydrazinopeptides in good yield and high purity. 相似文献
958.
959.
Sarazin F Savajols H Mittig W Nowacki F Orr NA Ren Z Roussel-Chomaz P Auger G Baiborodin D Belozyorov AV Borcea C Caurier E Dlouhy Z Gillibert A Lalleman AS Lewitowicz M Lukyanov SM de Oliveira F Penionzhkevich YE Ridikas D Sakurai H Tarasov O de Vismes A 《Physical review letters》2000,84(22):5062-5065
The masses of 31 neutron-rich nuclei in the range A = 29-47 have been measured. The precision of 19 masses has been significantly improved and 12 masses were measured for the first time. The neutron-rich Cl, S, and P isotopes are seen to exhibit a change in shell structure around N = 28. Comparison with shell model and relativistic mean field calculations demonstrate that the observed effects arise from deformed prolate ground state configurations associated with shape coexistence. Evidence for shape coexistence is provided by the observation of an isomer in 43S. 相似文献
960.
Dr. Stephanie A. Boer Luke Conte Dr. Andrew Tarzia Dr. Michael T. Huxley Dr. Michael G. Gardiner Dr. Dominique R. T. Appadoo Dr. Courtney Ennis Prof. Christian J. Doonan Assoc. Prof. Christopher Richardson Assoc. Prof. Nicholas G. White 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(57):e202201929
As hydrogen bonded frameworks are held together by relatively weak interactions, they often form several different frameworks under slightly different synthesis conditions and respond dynamically to stimuli such as heat and vacuum. However, these dynamic restructuring processes are often poorly understood. In this work, three isoreticular hydrogen bonded organic frameworks assembled through charge-assisted amidinium⋅⋅⋅carboxylate hydrogen bonds ( 1C/C , 1Si/C and 1Si/Si ) are studied. Three distinct phases for 1C/C and four for 1Si/C and 1Si/Si are fully structurally characterized. The transitions between these phases involve extreme yet recoverable molecular-level framework reorganization. It is demonstrated that these transformations are related to water content and can be controlled by humidity, and that the non-porous anhydrous phase of 1C/C shows reversible water sorption through single crystal to crystal restructuring. This mechanistic insight opens the way for the future use of the inherent dynamism present in hydrogen bonded frameworks. 相似文献