536 research outputs found

    Wear resistance of nano-polycrystalline diamond with various hexagonal diamond contents

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    Wear resistance of nano-polycrystalline diamond (NPD) rods containing various amounts of hexagonal diamond has been tested with a new method for practical evaluation of the wear–resistance rate of superhard ceramics, in addition to the measurements of their Knoop hardness. The wear resistance of NPD has been found to increase with increasing synthesis temperature and accordingly decreasing proportion of hexagonal diamond. A slight increase in Knoop hardness with the synthesis temperature also has been observed for these samples, consistent with the results of the wear–resistance measurements. These results suggest that the presence of hexagonal diamond would not yield any observable increase in both hardness and wear resistance of NPD, contradictory to a recent prediction suggesting that hexagonal diamond is harder than cubic diamond. It is also demonstrated that NPD is superior to single crystal diamond in terms of relatively homogeneous wearing without any significant chipping/cracking.Зносостійкість нано-полікристалічних алмазних (НПА) стрижнів, з різним вмістом гексагонального алмазу, була протестована новим методом практичної оцінки швидкості зносу надтвердої кераміки, додатково до вимірюваня їх твердості по Кнупу. Було виявлено, що зносостійкість НПА збільшується зі зростанням температури синтезу і, відповідно, зі зменшенням частки гексагональних алмазів. Також, відповідно до результатів вимірювань зносостійкості, для цих зразків спостерігалося невелике збільшення твердості по Кнупу з температурою синтезу. Ці результати дозволяють припустити, що присутність гексагональних алмазів не приводить до будь-якого помітного збільшення як твердості, так і зносостійкості НПА, що суперечить недавньому припущенню про те, що гексагональний алмаз твердіший, ніж кубічний. Також показано, що НПА перевершує монокристал алмазу з точки зору відносно однорідного зношування без значних відколів/тріщин.Износостойкость нано-поликристаллических алмазных (НПА) стержней, с различным содержанием гексагонального алмаза, была протестирована новым методом практической оценки скорости износа сверхтвердой керамики, в дополнение к измерениям их твердости по Кнупу. Было обнаружено, что износостойкость НПА увеличивается с ростом температуры синтеза и, соответственно, с уменьшением доли гексагональных алмазов. Также, в соответствии с результатами измерений износостойкости, для этих образцов наблюдалось небольшое увеличение твердости по Кнупу с температурой синтеза. Эти результаты позволяют предположить, что присутствие гексагональных алмазов не приводит к какому-либо заметному увеличению как твердости, так и износостойкости НПА, что противоречит недавнему предположению о том, что гексагональный алмаз тверже, чем кубический. Также показано, что НПА превосходит монокристалл алмаза с точки зрения относительно однородного изнашивания без значительных сколов/трещин

    Primary structure and spectroscopic studies of Neurospora copper metallothionein.

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    When Neurospora crassa is grown in the presence of Cu(II) ions, it accumulates the metal with the concomitant synthesis of a low molecular weight copper-binding protein. The molecule binds 6 g-atom of copper per mole protein (Mr = 2200) and shows a striking sequence homology to the zinc- and cadmium-binding vertebrate metallothioneins. Absorption, circular dichroism, and electron paramagnetic resonance spectroscopy of Neurospora metallothionein indicate the copper to be bound to cysteinyl residues as a Cu(I)-thiolate complex of the polymeric mu-thiolate structure [Cu(I)6RS7]-. This metal-binding mode is also in agreement with the unusual luminescence of the protein. Spectral perturbation studies with HgCl2 and p-(chloromercuri)benzoate suggest that the 6 Cu(I)ions are coordinated to the seven cysteinyl residues in the form of a single metal cluster. Neurospora apometallothionein is also capable of binding in vivo group IIB metal ions [Zn(II), Cd(II), and Hg(II)] as well as paramagnetic Co(II) ions with an overall metal-to-protein stoichiometry of 3. The spectroscopic properties of the fully substituted forms are indicative of a distorted tetrahedral coordination. However, metal titration of the apoprotein shows the third metal ion to be differently coordinated than the other two metal ions. This difference can be explained by the presence of only seven cysteine residues in Neurospora metallothionein as opposed to nine cysteine residues in the three-metal cluster of the mammalian metallothioneins

    On hydrogen bond correlations at high pressures

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    In situ high pressure neutron diffraction measured lengths of O H and H O pairs in hydrogen bonds in substances are shown to follow the correlation between them established from 0.1 MPa data on different chemical compounds. In particular, the conclusion by Nelmes et al that their high pressure data on ice VIII differ from it is not supported. For compounds in which the O H stretching frequencies red shift under pressure, it is shown that wherever structural data is available, they follow the stretching frequency versus H O (or O O) distance correlation. For compounds displaying blue shifts with pressure an analogy appears to exist with improper hydrogen bonds.Comment: 12 pages,4 figure

    Plume-lithosphere interaction, and the formation of fibrous diamonds

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    This work was financially supported though a JSPS international research fellowship PE 14721 (to MWB) and JSPS KAKENHI grant numbers JP 26287139 and JP15KK0150 (to HS). The work of DAZ and ALR was supported by Russian science foundation (16-17-10067). RB acknowledges funding from the NERC (NE/M000427/1). SM acknowledges funding from the NERC (NE/PO12167/1).Fluid inclusions in diamond provide otherwise inaccessible information on the origin and nature of carbonaceous fluid(s) in the mantle. Here we evaluate the role of subducted volatiles in diamond formation within the Siberian cratonic lithosphere. Specifically, we focus on the halogen (Cl, Br and I) and noble gas (He, Ne and Ar) geochemistry of fluids trapped within cubic, coated and cloudy fibrous diamonds from the Nyurbinskaya kimberlite, Siberia. Our data show Br/Cl and I/Cl ratios consistent with involvement of altered oceanic crust, suggesting subduction-derived fluids have infiltrated the Siberian lithosphere. 3He/4He ranging from 2 to 11 RA, indicates the addition of a primordial mantle component to the SCLM. Mantle plumes may therefore act as a trigger to re-mobilise subducted carbon-rich fluids from the sub-continental lithospheric mantle, and we argue this may be an essential process in the formation of fluid-rich diamonds, and kimberlitic magmatism.Publisher PDFPeer reviewe

    Submesothelial deposition of carbon nanoparticles after toner exposition: Case report

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    Inhalation of carbon nanoparticles (CNP) from toner dust has been shown to have impact on the respiratory health of persons exposed. Office printers are known emitters of CNP. We report about a female open office worker who developed weight loss and diarrhoea. Laparoscopy done for suspected endometriosis surprisingly revealed black spots within the peritoneum. Submesothelial aggregates of CNP with a diameter of 31-67 nm were found by scanning and transmission electron microscopy in these tissue specimens. Colon biopsies showed inflammatory bowel disease with typically signs of Crohn disease, but no dust deposits. Transport of CNP via lymphatic and blood vessels after inhalation in the lungs has to be assumed. In this case respiratory symptoms were not reported, therefore no lung function tests were done. We have shown that workers with toner dust exposure from laser printers can develop submesothelial deposition of CNP in the peritoneum. Impact of toner dust exposure on the respiratory health of office workers, as suspected in other studies, has to be evaluated further

    Investigation of structure and hydrogen bonding of super-hydrous phase B (HT) under pressure using first principles density functional calculations

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    High pressure behaviour of superhydrous phase B(HT) of Mg10Si3O14(OH)4 (Shy B) is investigated with the help of density functional theory based first principles calculations. In addition to the lattice parameters and equation of state, we use these calculations to determine the positional parameters of atoms as a function of pressure. Our results show that the compression induced structural changes involve cooperative distortions in the full geometry of the hydrogen bonds. The bond bending mechanism proposed by Hofmeister et al [1999] for hydrogen bonds to relieve the heightened repulsion due to short H--H contacts is not found to be effective in Shy B. The calculated O-H bond contraction is consistent with the observed blue shift in the stretching frequency of the hydrogen bond. These results establish that one can use first principles calculations to obtain reliable insights into the pressure induced bonding changes of complex minerals.Comment: 16 pages, 4 figure

    Apoptosis of Fashigh CD4+ synovial T cells by borrelia-reactive Fas-ligand(high) gamma delta T cells in Lyme arthritis

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    The function of the minor subset of T lymphocytes bearing the gamma delta T cell antigen receptor is uncertain. Although some gamma delta T cells react to microbial products, responsiveness has only rarely been demonstrated toward a bacterial antigen from a naturally occurring human infection. Synovial fluid lymphocytes from patients with Lyme arthritis contain a large proportion of gamma delta cells that proliferate in response to the causative spirochete, Borrelia burgdorferi. Furthermore, synovial gamma delta T cell clones express elevated and sustained levels of the ligand for Fas (APO-1, CD95) compared to alpha beta T cells, and induce apoptosis of Fashigh CD4+ synovial lymphocytes. The findings suggest that gamma delta T cells contribute to defense in human infections, as well as manifest an immunoregulatory function at inflammatory sites by a Fas-dependent process

    Neurons are MHC Class I-Dependent Targets for CD8 T Cells upon Neurotropic Viral Infection

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    Following infection of the central nervous system (CNS), the immune system is faced with the challenge of eliminating the pathogen without causing significant damage to neurons, which have limited capacities of renewal. In particular, it was thought that neurons were protected from direct attack by cytotoxic T lymphocytes (CTL) because they do not express major histocompatibility class I (MHC I) molecules, at least at steady state. To date, most of our current knowledge on the specifics of neuron-CTL interaction is based on studies artificially inducing MHC I expression on neurons, loading them with exogenous peptide and applying CTL clones or lines often differentiated in culture. Thus, much remains to be uncovered regarding the modalities of the interaction between infected neurons and antiviral CD8 T cells in the course of a natural disease. Here, we used the model of neuroinflammation caused by neurotropic Borna disease virus (BDV), in which virus-specific CTL have been demonstrated as the main immune effectors triggering disease. We tested the pathogenic properties of brain-isolated CD8 T cells against pure neuronal cultures infected with BDV. We observed that BDV infection of cortical neurons triggered a significant up regulation of MHC I molecules, rendering them susceptible to recognition by antiviral CTL, freshly isolated from the brains of acutely infected rats. Using real-time imaging, we analyzed the spatio-temporal relationships between neurons and CTL. Brain-isolated CTL exhibited a reduced mobility and established stable contacts with BDV-infected neurons, in an antigen- and MHC-dependent manner. This interaction induced rapid morphological changes of the neurons, without immediate killing or impairment of electrical activity. Early signs of neuronal apoptosis were detected only hours after this initial contact. Thus, our results show that infected neurons can be recognized efficiently by brain-isolated antiviral CD8 T cells and uncover the unusual modalities of CTL-induced neuronal damage

    CNS Recruitment of CD8+ T Lymphocytes Specific for a Peripheral Virus Infection Triggers Neuropathogenesis during Polymicrobial Challenge

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    Although viruses have been implicated in central nervous system (CNS) diseases of unknown etiology, including multiple sclerosis and amyotrophic lateral sclerosis, the reproducible identification of viral triggers in such diseases has been largely unsuccessful. Here, we explore the hypothesis that viruses need not replicate in the tissue in which they cause disease; specifically, that a peripheral infection might trigger CNS pathology. To test this idea, we utilized a transgenic mouse model in which we found that immune cells responding to a peripheral infection are recruited to the CNS, where they trigger neurological damage. In this model, mice are infected with both CNS-restricted measles virus (MV) and peripherally restricted lymphocytic choriomeningitis virus (LCMV). While infection with either virus alone resulted in no illness, infection with both viruses caused disease in all mice, with ∼50% dying following seizures. Co-infection resulted in a 12-fold increase in the number of CD8+ T cells in the brain as compared to MV infection alone. Tetramer analysis revealed that a substantial proportion (>35%) of these infiltrating CD8+ lymphocytes were LCMV-specific, despite no detectable LCMV in CNS tissues. Mechanistically, CNS disease was due to edema, induced in a CD8-dependent but perforin-independent manner, and brain herniation, similar to that observed in mice challenged intracerebrally with LCMV. These results indicate that T cell trafficking can be influenced by other ongoing immune challenges, and that CD8+ T cell recruitment to the brain can trigger CNS disease in the apparent absence of cognate antigen. By extrapolation, human CNS diseases of unknown etiology need not be associated with infection with any particular agent; rather, a condition that compromises and activates the blood-brain barrier and adjacent brain parenchyma can render the CNS susceptible to pathogen-independent immune attack
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