Adaptive remeshing for ductile fracture prediction in metal formingRemaillage adaptatif pour la prévision de la rupture ductile en mise en forme

The analysis of mechanical structures using the Finite Element Method in the framework of large elastoplastic strain, needs frequent remeshing of the deformed domain during computation. Indeed, the remeshing is due to the large geometrical distortion of finite elements and the adaptation to the physical behavior of the solution. This paper gives the necessary steps to remesh a mechanical structure during large elastoplastic deformations with damage. An important part of this process is constituted by geometrical and physical error estimates. The proposed method is integrated in a computational environment using the ABAQUS/Explicit solver and the BL2D-V2 adaptive mesher. To cite this article: H. Borouchaki et al., C. R. Mecanique 330 (2002) 709–716.     

华中五味子挥发性成份的研究

华中五味子有收敛、止咳、止汗、止泻、活血和健胃等作用。近年来已分离到约15种非挥发性成份,但关于它的挥发性成份迄今未见报道。我们用毛细管气相色谱法分离出     

Zinc porphyrin sensitized redox processes in microemulsions

Photoinduced electron transfer from Zn tetraphenylporphyrin to acceptors solubilized either in the lipid interior or aqueous bulk of anionic oil-in-water microemulsions has been investigated by nanosecond laser photolysis. While intimate cosolubilization appears to decrease the efficiency of electron transfer in the former, enhanced charge separation of the redox products has been observed in the latter.     

Vibrational spectra,normal coordinate analyses,and molecular configurations of crystalline propionic acid

Temperature dependence of the IR spectra of crystalline propionic acid were examined in the temperature range 242–50 K. The intensities of most absorption bands increased on lowering the temperature, but some bands diminished until they disappeared at temperatures lower than about 120 K. Normal coordinate analyses indicate that the former bands are due to the stable cis dimer and the latter due to the less stable trans dimer which would be produced from the cis dimer by simultaneous proton transfer along two hydrogen bonds.     

瓯柑石油醚提取物的GC-MS分析

为了研究瓯柑的挥发性成分和脂溶性成分, 采用GC-MS分析法进行分离鉴定, 并用面积归一法确定各成分的质量分数. 从瓯柑果肉石油醚提取物中分离鉴定出11种成分, 占总提取物的97.43%, 其主要成分为(Z, Z)-9, 12-十八碳二烯酸(37.46%)、γ-谷甾醇(22.91%);从瓯柑皮石油醚提取物中分离鉴定出10种成分, 占总提取物的99.79%, 其主要成分为柠檬烯(86.39%).     

HPLC of antibiotics. 1. Streptolydigin and related compounds

Two new acyltetramic acids related to streptolydigin have been isolated from fermentations of Streptomyces lydicus. The principal members of this complex were resolved by TLC on silica gel. However, the methods of detection, permanganate spray or bioautography, were not suitable for both crude fermentation broths and purified extracts. Gas chromatography is unsuitable for the detection of either underivatized or silylated streptolydigins. High performance liquid chromatography (HPLC) particularly on triethylaminoethyl cellulose is rapid and sensitive and is the method of choice for the analysis of both crude and purified samples. Using high performance liquid chromatography, two components were detected in the complex, which are not observed using any of the other chromatographic procedures.     

Degradation thermique et etude vibrationnelle de MII(NH4)4(P3O9)2x4H2O(M II=Cu2+, Ni2+, Co2+)

We have studied the thermal behaviour under atmospheric pressure of isotypic tetrahydrate cyclotriphosphates M^II(NH₄)₄(P₃O₉)₂x4H₂O (M ^II=Cu, Ni and Co), between 25 and 1400°C, by X-ray diffraction, thermal analyses (TG and DTA) and infrared spectrometry. This study shows that the series of the compounds M^II(NH₄)₄(P₃O₉)₂x4H₂O (M ^II=Cu, Ni and Co) after elimination of water, in two different stages, and ammonia leads, at 400°C to cyclotetraphosphate M₂ ^IIP₄O₁₂ crystallized and to a thermal residue with a formula H₄P₄O₁₂ which undergoes under a thermal degradation by evolving water and pentoxide phosphorus. The kinetic characteristics of the dehydration and elimination of ammonia have been determinated. The vibrational spectra of Cu(NH₄)₄(P₃O₉)₂x4H₂O were examined and interpreted, in the domain of the valency frequencies, on the basis of the crystalline structure of its isotypic compound Co(NH₄)₄(P₃O₉)₂x4H₂O whose cycle has the site symmetry C₁, of our results of the calculation of the IR frequencies and the successive isotopic substitutions of the equivalent atoms (3P, 3Oi and 6Oe belonging to the P₃Oi₃Oe₆ ring) of the P₃O₉ ³⁻ cycle with high symmetry D_3h. This revised version was published online in August 2006 with corrections to the Cover Date.     

Some difficulties for Clifton,Redhead, and Butterfield's recent proof of nonlocality

Clifton, Redhead, and Butterfield have recently produced a generalization of the new non-locality proof due to Greenberger, Horne, and Zeilinger. Their proof is intended to have certain advantages over the standard Belltype arguments. One of these is that, although the proof allows for causally relevant apparatus hidden variables, it avoids the need for making certain standard locality assumptions about those parameters. On closer inspection, the part of the proof which supposedly removes the need for such assumptions is shown to rest on a fallacy. This renders the proof invalid. Two other, related difficulties are explored along the way.1. CRB actually provide two nonlocality proofs, but our concern here is with the first.2. Cf. p.173 for a precise formulation of these. (Any references in these footnotes are to [1].) Note that, due to the way CRB define the µ's, these conditions are not entirely independent.3. Cf. p.174. Note that CRB claim to derive the independence of outcomes from apparatus existents via our other assumptions without imposing any other conditions on their distributions, citing Lemma 2, which we shall object to in Sec. 4 below. This should be given a careful reading; Lemma 2 only purports to derive the statistical independence of outcomes fromlocal (i.e., nearby) apparatus hidden variables. The independence of outcomes fromdistant apparatus hidden variables is assumed, rather, in OL.4. Here, and in many places, I shall rely on [1] for the details.5. CRB have endorsed this definition of M (personal correspondence).6. More precisely, those values of do so for at least one possible quadruple of apparatus existents, and measurement results; and foruncountably many setting quadruples in (p.167).7. Given CRB's way of defining the µ's so as to include the information found in the 's, the terms in OF and most of those in OL would actually be ill-defined in most cases (for each ) inany theory. This is simply because the measuring devices cannot be set to measure in two different directions at once. However, it should be possible to remedy that situation by simply redefining µ so that it includes only information about the state of the apparatus not covered by .8. CRB endorse the first of these two suggestions (personal correspondence).9. I have omitted the arguments fromA,B,C andD. Wherever they appear without arguments they will implicitly have the three with which they were first introduced. Note that M⁺ should ideally be indexed by and , as there is no reason to think that all the same members of M will makeABCD = +1 for different values of and .10. Cf. note 6 above.11. Note that in light of this objection to their proof, we can see that CRB also fail to establish the link they claim exists between TF, strict correlations, and the condition they call TF.TF is the four-particle analogue of the conjunction of Shimony's outcome independence and his parameter independence (p.162). They rest their claim about the link on Lemma 2 (pp.162 and 165).     

Conditional solubility versus pO2− of cerium(III) oxide in molten equimolar NaCl+KCl at 727°C

Reactions between cerium trichloride and oxide ions were studied in NaCl+KCl (1/1) at 1000°K, by potentiometry with a calcia-stabilized zirconia membrane electrode. Titration curves clearly demonstrated the existence of soluble cerium oxychloride (CeO⁺) and precipitated cerium oxide (Ce₂O₃), with respective dissociation constants 10^?11 and 10^?30 (molality scale). The corresponding conditional solubility diagram {log S (Ce^III)=f(pO^2?)} is presented and discussed.