Predicting ductile fracture of low carbon steel sheets: Stress-based versus mixed stress/strain-based Mohr–Coulomb model

Two distinct implementations of the Mohr–Coulomb failure model are used in conjunction with a non-associated quadratic plasticity model to describe the onset of fracture in low carbon steel sheets. The stress-based version corresponds to the original Mohr–Coulomb model in stress space. For the mixed stress/strain-based version, the Mohr–Coulomb failure criterion is first transformed into the space of stress triaxiality, Lode angle parameter and equivalent plastic strain and then used as stress-state dependent weighting function in a damage indicator model. Basic fracture experiments including tensile specimens of different notch radii and a punch test are performed to calibrate the material parameters of the respective models. Subsequently, the models are used to predict the crack initiation in a Hasek test and during the stamping of an anticlastic structure. Unlike for the calibration experiments, the loading history during stamping is highly non-linear. Both models can be calibrated with similar accuracy, but the strain-based model predicts the instant of onset of fracture with greater accuracy in the stamping experiment which is an advantage of the empirical damage accumulation rule.     

Ruthenium piano-stool complexes bearing imidazole-based PN ligands

A variety of piano-stool complexes of cyclopentadienyl ruthenium(II) with imidazole-based PN ligands have been synthesized starting from the precursor complexes [CpRu(C₁₀H₈)]PF₆, [CpRu(NCMe)₃]PF₆ and [CpRu(PPh₃)₂Cl]. PN ligands used are imidazol-2-yl, -4-yl and -5-yl phosphines.Depending on the ligand and precursor different types of coordination modes were observed; in the case of polyimidazolyl PN ligands these were κ¹P-monodentate, κ²P,N-, κ²N,N- and κ³N,N,N- chelating and μ-κP:κ²N,N-brigding. The solid-state structures of [CpRu(1a)₂Cl ]·H₂O (5^.H₂O) and [{CpRu(μ-κ²-N,N-κ’¹-P-2b)}₂](C₆H₅PO₃H)₂(C₆H₅PO₃H₂)_2, a hydrolysis product of the as well determined [{CpRu(2b)}₂](PF₆)₂^.2CH₃CN (7b^.2CH₃CN) were determined (1a = imidazol-2-yldiphenyl phosphine, 2b = bis(1-methylimidazol-2-yl)phenyl phosphine, 3a = tris(imidazol-2-yl)phosphine). Furthermore, the complexes [CpRu(L)₂]PF₆ (L = imidazol-2-yl or imidazol-4-yl phosphine) have been screened for their catalytic activity in the hydration of 1-octyne.     

Chiral separation of cathinone derivatives used as recreational drugs by cyclodextrin-modified capillary electrophoresis

In recent years, cathinone derivatives have entered the global drug market and caused serious social problems in many European countries. Modification of the basic structure of cathinone leads to a multitude of derivatives, including the most popular representative mephedrone. All those substances contain a stereogenic center and therefore two isoforms exist. As it is the case with many chiral active pharmaceutical ingredients, even the pharmacological effect of the enantiomers of those psychoactive compounds may differ. During this research, an easy-to-prepare chiral capillary zone electrophoresis method for the enantioseparation of a set of 19 cathinone derivatives was developed. Testing different types of cyclodextrin (CD), including native-β-CD, carboxymethyl-β-CD, 2-hydroxypropyl-β-CD, sulfated-β-CD, and native γ-CD, best results were obtained with the negatively charged sulfated-β-CD. The effect of the CD concentration, the temperature, and the addition of ACN to the BGE on the enantioseparation is shown by three model compounds. Under optimal conditions, using 20 mg/mL sulfated-β-CD in 50 mM ammonium acetate buffer pH?= 4.5 containing 10% v/v ACN at a cassette temperature of 40°C and with an applied voltage of 20 kV, all derivatives except methedrone were resolved in their enantiomers within 20 min.     

Large deformation of anisotropic austenitic stainless steel sheets at room temperature: Multi-axial experiments and phenomenological modeling

A newly developed multi-axial testing technique for sheet materials is employed to investigate the inelastic response of a temper-rolled stainless steel 301LN under isothermal quasi-static loading conditions at room temperature. The experimental technique consists of a flat sheet specimen, which is subject to combinations of shear and normal loading using a custom-made dual-actuator system. The large deformation behavior under monotonic loading is determined along more than 20 distinct radial paths in the stress space. The experimental results indicate that Hill's quadratic yield function along with an associated flow rule provides a good approximation of the initial yield behavior of this anisotropic two-phase FCC/BCC sheet material. Based on the experimental data for radial monotonic loading, it is concluded that conventional isotropic-kinematic hardening models cannot successfully describe the strain hardening of this austenitic steel. Instead, a non-associated anisotropic hardening model is proposed that relates the increase in yield strength to an isothermal martensitic transformation kinetics law. The comparison of the model predictions with the experimental results shows very good agreement for all biaxial and uniaxial experiments.     

A Synthetic Route Toward Tetrazoles: The Thermolysis of Geminal Diazides

A new synthetic route toward the tetrazole core is described, which is based on a general fragmentation pattern that was found in a range of compounds featuring geminal diazido units. Through a simple two-step procedure, the synthesis of structurally diverse target compounds containing a tetrazole, such as tetrazoloquinoxalinones, benzoylaryltetrazoles, tetrazolotriazinones, and tetrazoloazepinones, was easily accomplished, starting from broadly accessible substrates (i.e., oxindoles, diarylethanones, pyrazolones, and phenanthrols). The initial oxidative diazidation reaction with iodine and sodium azide under mild conditions is followed by the thermal fragmentation under microwave irradiation, leading to the tetrazole products. Noteworthy, an experimental solution is presented in which the potentially hazardous diazide intermediates are not isolated and the concentration of crude reaction mixtures containing diazides is not required to achieve the tetrazoles in good yields.     

Comments on `Correction of Maxwell's equations for signals I andII' [by R.J. Mohr]

The commenter states that Harmuth's (see ibid., vol.28, no.4, p.250, 1986) characterization of Godel's (1931) work is incorrect, or, at the very best, extremely misleading. He also states that Godel did not show, as Harmuth claims, that every statement cannot be proven and that they can only be disproven using counterexample     

APPEARANCE OF PHOTOPHOSPHORYLATION CAPACITY: THRESHOLD vs GRADED CONTROL BY PHYTOCHROME

Abstract— It is shown that in attached mustard cotyledons graded control of chlorophyll synthesis by physiologically active phytochrome (P_fr) and threshold control by P_fr of the 'potential capacity' to photophosphorylate are totally different phytochrome actions even though both controls are essential for the build-up of the same functional complex, the machinery for photophosphorylation. The essential findings are as follows: The action of P_fr (made by a 1 min red light pulse) on the capacity and efficiency of photophosphorylation is rapid—detectable after 15 min and completed after 30 min—whereas the action of P_fr on chlorophyll formation is slower—only detectable 45 min after the original red light pulse (R). Detailed escape studies (loss of full reversibility of the inductive effect of a R pulse by far-red) show that the effect of a R pulse on chlorophyll synthesis remains fully reversible for 45 min whereas the action of P_fr on the capacity for photophosphorylation is very fast (occurring within 2 min). Control of capacity for photophosphorylation is a threshold response (whereby the threshold value is approximately 1.25% P_fr based on total phytochrome at 36 h = 100%) whereas control by P_fr of chlorophyll synthesis is graded. Control of capacity for photophosphorylation by P_fr only operates if the hypocotyl hook is connected to the cotyledons for at least 2 min after the inductive R pulse, i.e. until full escape from reversibility has occurred, whereas chlorophyll formation in the cotyledons is not affected by the separation of hook and cotyledons.     

STIMULATION OF APPEARANCE OF EXTRAPLASTIDIC TETRAPYRROLES BY A PHOTOOXIDATIVE TREATMENT OF THE PLASTIDS*

In the mustard seedling (Sinapis alba L.) the appearance of photodetectable phytochrome and synthesis of relatively abundant cytosolic hemoproteins (nitrite reductase, ascorbate peroxidase) are stimulated rather than impaired by a photooxidative treatment of the plastids. While the ability to synthesize protoporphyrin IX from exogenous 5-aminolevulinic acid was preserved in the photooxidatively damaged plants, protochlorophyll and chlorophyll accumulation was no longer possible. It appears from our data that in higher plants the pathway of tetrapymole synthesis up to protoporphyrin IX is not adversely affected by a photooxidative treatment of the plastids that destroys the capacity of the organelle to synthesize chlorophyll.     

Ueber die Ermittelung freier Minerals?uren

Ohne Zusammenfassung