Identification of ritual blood in African artifacts using TOF-SIMS and synchrotron radiation microspectroscopies

A new protocol is implemented to demonstrate the presence of blood in the patina of African art objects from Mali. Divided into three steps, the protocol first consists in demonstrating the presence of proteins and localizing them in the sample's cross sections using time-of-flight secondary ion mass spectrometry (TOF-SIMS) and synchrotron-based infrared microspectrometry (microFT-IR). In a second time, TOF-SIMS is used to investigate heme, which is a blood marker. If heme is missing, which could mean that it is too degraded to be detected, X-ray microfluorescence (microXRF) and X-ray absorption near-edge microspectroscopy (microXANES) are used to prove the presence of iron in the protein area and to get a fingerprint of its chemical environment. This permits us thus to demonstrate that iron is indeed linked with proteins and not with mineral phases of the sample. Coupled with the ritual context of the objects, this constitutes a proof of the use of blood. Thanks to this protocol, which has the major advantage of avoiding false positive results, the presence of blood has been demonstrated in seven out of the eight studied samples.     

Dark-capacitance transients in MIS tunnel diodes

Dark-capacitance transients in MIS tunnel diodes switched from accumulation to deep depletion depend on the interface state occupancy. This time dependent function is derived and its behavior described for electron emission and electron-hole pair generation with tunneling and thermally controlled occupancies. A new method of determining the tunneling relaxation time constant τ_T from the electron emission transient at low temperature is described. Measurements of MIS tunnel diodes with oxide thickness d_ox = 17 to 80 Å agree with theory and the resultant values of τ_T compare with previously reported results from photocapacitance[2].     

Why models rather than rules give a better account of propositional reasoning: A reply to Bonatti and to O'Brien, Braine, and Yang.

D. P. O'Brien et al (see record 1995-08272-001) argue that the mental model theory of propositional reasoning is easy to refute, and they report 3 experiments that they believe falsify the theory. In contrast, L. Bonatti (see record 1995-08253-001) argues that the model theory is too flexible to be falsified. It is shown that the experiments by O'Brien et al do not refute the model theory and that Bonatti's claims are ill founded. Formal rule theories of propositional reasoning have 3 major weaknesses in comparison with the model theory: (1) They have no decision procedure; (2) they lack predictive power, providing no account of several robust phenomena (e.g., erroneous conclusions tend to be consistent with the premises); and (3) as a class of theories, they are difficult to refute experimentally. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Experimental and calculated liquid-liquid interfacial tension in demixing metal alloys

Liquid-liquid interracial tension in binary and temary Al-based monotectic systems has been determined experimentally with a tensiometric method in a wide temperature interval. The temperature dependence of the interfacial tension is well described by a power law function of the type σαβ - （1 - T/Tc）δ with the critical exponent δ= 1.3 and a critical temperature Tc. Theoretical models describing the liquid-liquid interface in monotectic alloys and their applicability for calculation of the interfacial tension and its temperature dependence in binary systems are considered.     

Reaktionen mit Cyclobutendionen. LII. Reaktionen von 4-Hydroxy-3-phenyl-cyclobut-(3)-en-onen-(1) mit Arylhydrazinen

Reactions of Cyclobutendiones. LII. Reaction of 4-Hydroxy-3-phenyl-3-cyclobuten-1-ones with Arylhydrazines In the reaction of hydroxycyclobutenones of the typ 1 – 4 with arylhydrazines 5 an unexpected reaction behaviour is found. The major products are hydrazones of different structure, the well known hydroxy-cyclopropane-carboxylicacid hydrazines 6 [1] are byproducts. The direction of the reaction depends on the substituents X, on the different substituted arylhydrazines and the solvents.     

The manufacture of high-value carbon from coal-tar pitch

World-wide, 17 million ta^?1 of coal-tar are obtained as a by product in the chamber coking process for the production of metallurgical coke. Refining of this aromatic raw material yields coal-tar pitch which is the traditional coal-derived starting material for the manufacture of carbon precursors and carbon artefacts. Considerable progress has been made in the elucidation of the physical and chemical nature of this material by means of chromatography, n.m.r. spectroscopy, thermal analysis and chemical reactions schemes. The dominant fields of application of pitch are the manufacture of pitch coke and electrode binders. Delayed coking and horizontal chamber coking are the technologies currently used for the production of cokes with low sulphur and metal content, for anodes for the aluminium-refining industry and the electric steel process. Coal-tar pitch, low in quinoline-insolubles (QI), is an excellent raw material for the manufacture of needle-cokes with a low coefficient of thermal expension (CTE). The separation of inherent QI can be performed via gravity settling in aliphatic hydrocarbon mixtures, by centrifugation in a disc separator or by filtration. The possible co-carbonization with aromatic petroleum-derived residues yields premium coke suitable for the manufacture of UHP-electrodes. New developments in the production of coke from coal-tar pitch aim to improve coke yields and increase anisotropy (i.e. low CTE and high electrical conductivity values). Further technological progress has been made in the manufacture of hard pitch which can be used as a starting material for the production of pitch coke in the chamber coking process and for the production of electrode binders by means of a continuous flash process with optimized thermal and pressure treatment of pitch, thus facilitating the ‘tailored’ manufacture of binder pitches of different qualities.     

NMR structure of the (+)-CPI-indole/d(GACTAATTGAC)-d(GTCAATTAGTC) covalent complex

We report the NMR solution structure of (+)-CPI-indole (CPI, 1,2,8,8a-tetrahydrocyclopropa[c]pyrrolo[3,2-e]indol-4(5H)-one), an agent belonging to the CC-1065/duocarmycin family of antitumor compounds. This (+)-CPI-indole structure is covalently bound to d(G(1)ACTAATTGTC(11))-d(G(12)TCAATTAGTC(22)), a synthetic DNA duplex containing a high-affinity binding site. The three-dimensional structure has been determined by several cycles of restrained molecular dynamics calculations with a total of 563 NMR-derived constraints, both in vacuo and by using the generalized Born solvent continuum model. In-depth analysis of the structure of this ligand-DNA complex led to a detailed knowledge of the bound state conformation of the CPI-indole, the most simplified agent related to CC-1065 and duocarmycins, the parent members of a family of extremely potent antitumor compounds. Comparison of the CPI-indole bound conformation with those previously found for (+)-duocarmycin SA (DSA), its unnatural enantiomer (-)-DSA, and the demethoxylated analogue (+)-DSI in their DNA complexes provided additional evidence of the tight correlation between the catalytic effect exerted by DNA on the alkylation reaction and the extent of angular twist between the two planar heteroaromatic subunits of these agents. Additionally, comparison of the structural features of the DNA-bound state of a "naked" ligand, such as CPI-indole, with those of various other duocarmycin agents provided useful information for the interpretation of the observed effects on chemical reactivity of the different substitution patterns at the hemispheres of these types of complex.     

Polyurethane‐infiltrated carbon foams: A coupling of thermal and mechanical properties

The thermal and mechanical properties of polyurethane‐infiltrated carbon foam of various densities were investigated. By combining the high thermal conductivity of the carbon foam with the mechanical toughness of the pure polyurethane, a mechanically tough composite (relative to the unfilled foam) that could be used at higher temperatures than the polyurethane's degradation was formed. Both the tensile strength and the modulus increased by an order of magnitude for the composites compared to unfilled foam, while the compressive and shear strengths and moduli of the composites approached values exhibited by pure polyurethane. At both 300 and 400°C, the rectangular blocks of pure polyurethane lost their mechanical integrity due to decomposition in air. Thermogravimetric analysis confirms substantial initial weight loss above 290°C. Filled carbon foam blocks, however, maintain their mechanical integrity at both 300 and 400°C indefinitely, although the bulk of the rectangular block mass is polyurethane. Three different carbon foam densities are examined. As expected, the higher density foams show greater heat transfer. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 2348–2355, 2003