3,788 research outputs found

    A Nonpolymorphic Class I Gene in the Murine Major Histocompatibility Complex

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    DNA sequence analysis of a class I gene (QlO), which maps to the Qa2,3 locus in the C57BL/lO (H- 2b haplotype) mouse, reveals that it is almost identical to a cDNA clone (pH16) isolated from a SWR/J (H-2q haplotype) mouse liver cDNA library. Exon 5, in particular, has an unusual structure such that a polypeptide product is unlikely to be anchored in the cell membrane. Our findings suggest that the two sequences are derived from allelic class I genes, which are nonpolymorphic, in contrast to H-2K allelic sequences from the same mice, and they may encode liver-specific polypeptides of unknown function. Our previous studies indicate that the QlO gene is a potential donor gene for the generation of mutations at the H-2K locus by inter-gene transfer of genetic information. Thus the lack of polymorphism in class I genes at the QlO locus implies either that they are not recipients for such exchanges or that selective pressure prevents the accumulation of mutations in genes at this locus

    Acquiring OS X File Handles through Forensic Memory Analysis

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    Memory analysis has become a critical capability in digital forensics because it provides insight into system state that cannot be fully represented through traditional media analysis. The volafox open source project has begun the work of structured memory analysis for OS X with support for a limited set of kernel structures. This paper addresses one memory analysis deficiency on OS X with the introduction of a new volafox module for parsing file handles associated with running processes. The developed module outputs information comparable to the UNIX lsof (list open files) command, which is used to validate the results

    Degradation studies of crosslinked polyethylene. 1, Aged in air

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    Silane crosslinking of polyethylene, carried out by grafting an organofunctional silane (vinyltrimethoxysilane) onto polyethylene and by subsequent moisture crosslinking in hot water using a tin catalyst, has been widely used in industrial applications because of its advantages in terms of low cost and easy processing. This study focused on the degradation processes which occurred in the material after air ageing in an oven; temperatures ranged from 90 to 220°C, while ageing times ranged from 2h to 500h. Significant structural changes were observed according to the different ageing conditions (below and above the melting region of the material), since the carbonyl group concentration increased substantially during ageing above the melting region and the silicone containing groups were also affected by the degradation. These structural changes affected the mechanical and thermal properties of the material, which was annealed at lower ageing temperatures (up to 155°C) and highly degraded at higher temperatures, when C-C crosslinks formed. Experimental design software was used in order to optimise the number of experimental trials and to model the results obtained; its analysis contributed to the interpretation of the results

    Degradation studies of crosslinked polyethylene. 2, Aged in water

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    Silane crosslinking of polyethylene was carried out by grafting an organofunctional silane (vinyltrimethoxysilane) onto polyethylene and by subsequent moisture crosslinking in hot water using a tin catalyst. This study focuses on the degradation processes, which occurred in the material after water ageing in an autoclave; ageing temperatures ranged from 90 to 190°C, while ageing times ranged from 2h to 500h. Significant changes in the chemical structure of the material were observed by FTIR, as carbonyl group concentration increased and different structures formed in the region of absorbance of groups containing silicone; the structural changes affected significantly the mechanical properties as shown by the tensile data. A chemical analysis of the extracts in chloroform of water aged samples carried out by using FTIR, LIMA and GPC techniques and some optical microscopy evidence, suggested that the mechanism of degradation in water is different from the one in air, as during water ageing the antioxidants are washed away by water and hydrolytic oxidation also occurs. ECHIP experimental design software was used in order to optimise the number of experimental trials and to model the results obtained. Keywords: PE-crosslink, water ageing, carbonyl ratio, silane, antioxidants

    Barriers to the Effective Adhesion of High-Density Hardwood Timbers for Glue-Laminated Beams in Australia

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    A number of international timbers of high commercial importance are extremely difficult to glue, which is significantly hindering access to global market opportunities for engineered wood products, especially for heavily demanded structural products. Some particularly problematic timbers in Australia are the dominant commercial hardwood species, including spotted gum (Corymbia spp.) and Darwin stringybark (Eucalyptus tetrodonta). These species are renowned for their very high mechanical properties, natural durability and attractive aesthetic appeal. However, they are notoriously difficult to glue, especially for sawn laminate-based engineered wood products, such as structural glue-laminated beams. Despite considerable effort and testing of diverse internationally established best-practice approaches to improve adhesion, glue-laminated beam samples of these timbers still frequently fail to meet the requirements of the relevant standard, mainly due to excessive glue line delamination. This paper discusses the key barriers to effective adhesion of these high-density timbers and particularly emphasises the necessity of achieving greater adhesive penetration. Greater adhesive penetration is required to enhance mechanical interlocking, entanglement and molecular interactions between the adhesive and the wood to achieve stronger and more durable bonds. Potential solutions to enhance adhesive penetration, as well as to improve gluability in general, are discussed in terms of their likelihood to satisfactorily prevent delamination and the potential to be applied at an industrial scale. This new fundamental understanding will assist the development of solutions, allowing industry to commercialise newly engineered wood products made from high-density timbers

    Magneto-optical Kerr Effect Studies of Square Artificial Spin Ice

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    We report a magneto-optical Kerr effect study of the collective magnetic response of artificial square spin ice, a lithographically-defined array of single-domain ferromagnetic islands. We find that the anisotropic inter-island interactions lead to a non-monotonic angular dependence of the array coercive field. Comparisons with micromagnetic simulations indicate that the two perpendicular sublattices exhibit distinct responses to island edge roughness, which clearly influence the magnetization reversal process. Furthermore, such comparisons demonstrate that disorder associated with roughness in the island edges plays a hitherto unrecognized but essential role in the collective behavior of these systems.Comment: Physical Review B, Rapid Communications (in press

    Solid Solid Phase Transitions and tert-Butyl and Methyl Group Rotation in an Organic Solid: X-ray Diffractometry, Differential Scanning Calorimetry, and Solid-State H-1 Nuclear Spin Relaxation

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    Using solid state 1H nuclear magnetic resonance (NMR) spin-lattice relaxation experiments, we have investigated the effects of several solid-solid phase transitions on t-butyl group and methyl group rotation in solid 1,3,5-tri-t-butylbenzene. The goal is to relate the dynamics of the t-butyl groups and their constituent methyl groups to properties of the solid determined using single-crystal X-ray diffraction and differential scanning calorimetry (DSC). On cooling, the DSC experiments see a first-order, solid-solid phase transition at either 268 K or 155 K (but not both) depending on thermal history. The 155 K transition (on cooling) is identified by single-crystal X-ray diffraction to be one from a monoclinic phase (above 155 K) where the t-butyl groups are disordered (that is, with a rotational six-fold intermolecular potential dominating) to a triclinic phase (below 155 K) where the t-butyl groups are ordered (that is, with a rotational threefold intermolecular potential dominating). This transition shows very different DSC scans when both a 5 mg polycrystalline sample and a 19 mg powder sample are used. The 1H spin-lattice relaxation experiments with a much larger 0.7 g sample are very complicated and, depending on thermal history, can show hysteresis effects over many hours and over very large temperature ranges. In the high-temperature monoclinic phase, the t-butyl groups rotate with NMR activation energies (closely related to rotational barriers) in the 17-23 kJ mol-1 range and the constituent methyl groups rotate with NMR activation energies in the 7-12 kJ mol-1 range. In the lowtemperature triclinic phase, the rotations of the t-butyl groups and their methyl group in the aromatic plane are quenched (on the NMR time scale). The two out-of-plane methyl groups in the t-butyl groups are rotating with activation energies in the 5-11 kJ mol-1 range

    Solid Solid Phase Transitions and tert-Butyl and Methyl Group Rotation in an Organic Solid: X-ray Diffractometry, Differential Scanning Calorimetry, and Solid-State H-1 Nuclear Spin Relaxation

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    Using solid state 1H nuclear magnetic resonance (NMR) spin-lattice relaxation experiments, we have investigated the effects of several solid-solid phase transitions on t-butyl group and methyl group rotation in solid 1,3,5-tri-t-butylbenzene. The goal is to relate the dynamics of the t-butyl groups and their constituent methyl groups to properties of the solid determined using single-crystal X-ray diffraction and differential scanning calorimetry (DSC). On cooling, the DSC experiments see a first-order, solid-solid phase transition at either 268 K or 155 K (but not both) depending on thermal history. The 155 K transition (on cooling) is identified by single-crystal X-ray diffraction to be one from a monoclinic phase (above 155 K) where the t-butyl groups are disordered (that is, with a rotational six-fold intermolecular potential dominating) to a triclinic phase (below 155 K) where the t-butyl groups are ordered (that is, with a rotational threefold intermolecular potential dominating). This transition shows very different DSC scans when both a 5 mg polycrystalline sample and a 19 mg powder sample are used. The 1H spin-lattice relaxation experiments with a much larger 0.7 g sample are very complicated and, depending on thermal history, can show hysteresis effects over many hours and over very large temperature ranges. In the high-temperature monoclinic phase, the t-butyl groups rotate with NMR activation energies (closely related to rotational barriers) in the 17-23 kJ mol-1 range and the constituent methyl groups rotate with NMR activation energies in the 7-12 kJ mol-1 range. In the lowtemperature triclinic phase, the rotations of the t-butyl groups and their methyl group in the aromatic plane are quenched (on the NMR time scale). The two out-of-plane methyl groups in the t-butyl groups are rotating with activation energies in the 5-11 kJ mol-1 range
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