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101.
In this work, the simulation of earings in cup drawing by means of a recently developed anisotropic combined hardening material model is discussed. The model represents a multiplicative formulation of anisotropic elastoplasticity in the finite strain regime with nonlinear kinematic and isotropic hardening. Plastic anisotropy is described by the use of second-order structure tensors as additional arguments in the representation of the yield function and the plastic flow rule. The evolution equations are integrated by a form of the exponential map that preserves the plastic volume and the symmetry of the internal variables. Finite element simulations of cylindrical cup drawing processes are performed by means of ABAQUS/Standard where the discussed material model has been implemented into a user-defined reduced integration solid-shell element. (© 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
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The extraction of stoichiometric ternary K/Si/P, K/Ge/P, and K/Si/As solid mixtures with en/crypt‐222 afforded compounds with binary anions of the respective groups 14/15 elemental combination. Although the analysis of the products turned out to be extremely difficult owing to their intrinsically poor crystallinity and low solubility, we have evidence that one of them contains (SiP6H2)2– anions. Preliminary data from the two other compounds indicate the existence of the heavier Ge/P and Si/As variants as well. The combination of all analytical results, including X‐ray crystallography, energy‐dispersive X‐ray (EDX) spectroscopy, electrospray ionization mass spectrometry (ESI‐MS), and nuclear magnetic resonance (NMR) spectroscopy, point towards the named composition of the anions and their doubly protonated nature. By this, they represent the first binary Zintl anions of the Si/P and Si/As elemental combination and complement the recent endeavors to synthesize binary Zintl anions of the light(er) p‐block elements. We discuss our attempts to elucidate the clusters' identity and provide our results as the most probable interpretation of the data, additionally corroborated by quantum chemical analyses. 相似文献
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Conrad A. P. Goodwin Jing Su Thomas E. Albrecht‐Schmitt Anastasia V. Blake Enrique R. Batista Scott R. Daly Stefanie Dehnen William J. Evans Andrew J. Gaunt Stosh A. Kozimor Niels Lichtenberger Brian L. Scott Ping Yang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(34):12050-12050
105.
Niels Lichtenberger Werner Massa Stefanie Dehnen 《Angewandte Chemie (International ed. in English)》2019,58(10):3222-3226
We present the results from a reactivity study of the binary anion (TlBi3)2? towards Group 12 metal compounds MPh2 (M=Zn, Cd, Hg) to gain access to coordination compounds of polycyclic polypnictide molecules such as Bi73? or Bi113?. The coordination chemistry of these polybismuthide cages has been unprecedented to date, while it has been known for a long time for the lighter Group 15 anions Pn73? (Pn=P, As, Sb). The use of (TlBi3)2?, previously shown to release Tl under certain conditions in situ, resulted in the formation of the first heterometallic polyanion in which a nortricyclane‐type polybismuthide coordinates a transition‐metal atom, [(Bi7)Cd(Bi7)]4?. Reactions with the lighter Group 12 metal precursor yielded the uncommon ternary cluster [(Bi6)Zn3(TlBi5)]4?, most likely representing a reaction intermediate, and at the same time hinting at the formation of the nortricyclane‐shaped cage. Quantum‐chemical studies provide deeper insight into the stability trends of the [(E7)M(E7)]4? anion family and reveal a complex bonding situation in [(Bi6)Zn3(TlBi5)]4?, which features both localized and multi‐center bonding. 相似文献
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Control of reaction mechanisms in cationically polymerized epoxy resins facilitates the adjustment of morphology and mechanical properties 下载免费PDF全文
André Arnebold Florian Plander Karsten Thiel Stefanie Wellmann Andreas Hartwig 《Journal of Polymer Science.Polymer Physics》2016,54(21):2188-2199
Structure–property relations of cationically polymerized epoxy thermosets with different morphologies are examined. The morphology adjustment of amorphous epoxy based copolymers and partially crystalline polymer alloys is carried out with star‐shaped poly(ε‐caprolactone) (SPCL) bearing various numbers of hydroxyl end groups. These hydroxyl groups are known for their reactivity toward epoxides following the activated monomer (AM) mechanism. For this reason, four‐armed SPCL was synthesized with four hydroxyl end groups (SPCL‐tetraol) and, in addition, with successively esterified ones down to a SPCL with four ester end groups (SPCL‐tetraester). SPCL species bearing fewer or no hydroxyl end groups segregate into needle‐like nanodomains within the epoxy networks and, if the concentration is high enough, also into crystalline domains. The stronger phase separation of SPCL‐tetraester within the epoxy network compared with SPCL‐tetraol is due to a reduction of the AM mechanism. The mechanical properties resulting from different morphologies lead to a trade‐off between higher storage moduli and Tg values in the case of the more phase separated (and partially crystalline) polymer alloys and higher strain at break in the case of the amorphous copolymers. Nevertheless, in both cases toughness is improved or at least kept on the same level as for the pure epoxy resin. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 2188–2199 相似文献
109.
Niklas Rinn Dr. Jens P. Eußner Willy Kaschuba Dr. Xiulan Xie Prof. Dr. Stefanie Dehnen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(9):3094-3104
Reactions of R1SnCl3 (R1=CMe2CH2C(O)Me) with (SiMe3)2Se yield a series of organo‐functionalized tin selenide clusters, [(SnR1)2SeCl4] ( 1 ), [(SnR1)2Se2Cl2] ( 2 ), [(SnR1)3Se4Cl] ( 3 ), and [(SnR1)4Se6] ( 4 ), depending on the solvent and ratio of the reactants used. NMR experiments clearly suggest a stepwise formation of 1 through 4 by subsequent condensation steps with the concomitant release of Me3SiCl. Furthermore, addition of hydrazines to the keto‐functionalized clusters leads to the formation of hydrazone derivatives, [(Sn2(μ‐R3)(μ‐Se)Cl4] ( 5 , R3=[CMe2CH2CMe(NH)]2), [(SnR2)3Se4Cl] ( 6 , R2=CMe2CH2C(NNH2)Me), [(SnR4)3Se4][SnCl3] ( 7 , R4=CMe2CH2C(NNHPh)Me), [(SnR2)4Se6] ( 8 ), and [(SnR4)4Se6] ( 9 ). Upon treatment of 4 with [Cu(PPh3)3Cl] and excess (SiMe3)2Se, the cluster fragments to form [(R1Sn)2Se2(CuPPh3)2Se2] ( 10 ), the first discrete Sn/Se/Cu cluster compound reported in the literature. The derivatization reactions indicate fundamental differences between organotin sulfide and organotin selenide chemistry. 相似文献
110.