368 research outputs found

    Performance of a Functionalised Polymer-Coated Silica at Treating Uranium Contaminated Groundwater from a Hungarian Mine Site

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    The performance of an active material for treating uranium contaminated groundwater within a permeable reactive barrier (PRB) is reported. This material, called PANSIL, has a tailored ligand system that selectively removes the uranyl (UO22+) cation from solution. The active uranyl ligand in PANSIL is a polyacryloamidoxime resin derived from polyacrylonitrile, which is deposited from solution onto the surface of quartz sand to form a thin film coating. PANSIL is effective at sequestering cationic and neutral uranyl species when the solution pH is above 4, due to the stability of the polyacryloamidoxime-uranyl complex formed. However the rate of sequestration decreases rapidly when the pH exceeds about 8 where neutral uranyl species are present only at very low concentrations. It can preferentially sequester UO22+ in the presence of typical divalent groundwater cations. In mildly alkaline conditions the sequestration performance in groundwater is sensitive to the concentration of uranyl complexing ligands, such as bicarbonate. Such behaviour has important consequences for PRB design as it will determine the barrier thickness required to treat a particular groundwater flow rate

    Numerical semigroups with large embedding dimension satisfy Wilf's conjecture

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    We give an affirmative answer to Wilf's conjecture for numerical semigroups satisfying 2 \nu \geq m, where \nu and m are respectively the embedding dimension and the multiplicity of a semigroup. The conjecture is also proved when m \leq 8 and when the semigroup is generated by a generalized arithmetic sequence.Comment: 13 page

    On the characteristic connection of gwistor space

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    We give a brief presentation of gwistor space, which is a new concept from G_2 geometry. Then we compute the characteristic torsion T^c of the gwistor space of an oriented Riemannian 4-manifold with constant sectional curvature k and deduce the condition under which T^c is \nabla^c-parallel; this allows for the classification of the G_2 structure with torsion and the characteristic holonomy according to known references. The case with the Einstein base manifold is envisaged.Comment: Many changes since first version, including title; Central European Journal of Mathematics, 201

    The Complexity of the Empire Colouring Problem

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    We investigate the computational complexity of the empire colouring problem (as defined by Percy Heawood in 1890) for maps containing empires formed by exactly r>1r > 1 countries each. We prove that the problem can be solved in polynomial time using ss colours on maps whose underlying adjacency graph has no induced subgraph of average degree larger than s/rs/r. However, if s≄3s \geq 3, the problem is NP-hard even if the graph is a forest of paths of arbitrary lengths (for any r≄2r \geq 2, provided s<2r−(2r+1/4+3/2)s < 2r - \sqrt(2r + 1/4+ 3/2). Furthermore we obtain a complete characterization of the problem's complexity for the case when the input graph is a tree, whereas our result for arbitrary planar graphs fall just short of a similar dichotomy. Specifically, we prove that the empire colouring problem is NP-hard for trees, for any r≄2r \geq 2, if 3≀s≀2r−13 \leq s \leq 2r-1 (and polynomial time solvable otherwise). For arbitrary planar graphs we prove NP-hardness if s<7s<7 for r=2r=2, and s<6r−3s < 6r-3, for r≄3r \geq 3. The result for planar graphs also proves the NP-hardness of colouring with less than 7 colours graphs of thickness two and less than 6r−36r-3 colours graphs of thickness r≄3r \geq 3.Comment: 23 pages, 12 figure

    Size Doesn't Matter: Towards a More Inclusive Philosophy of Biology

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    notes: As the primary author, O’Malley drafted the paper, and gathered and analysed data (scientific papers and talks). Conceptual analysis was conducted by both authors.publication-status: Publishedtypes: ArticlePhilosophers of biology, along with everyone else, generally perceive life to fall into two broad categories, the microbes and macrobes, and then pay most of their attention to the latter. ‘Macrobe’ is the word we propose for larger life forms, and we use it as part of an argument for microbial equality. We suggest that taking more notice of microbes – the dominant life form on the planet, both now and throughout evolutionary history – will transform some of the philosophy of biology’s standard ideas on ontology, evolution, taxonomy and biodiversity. We set out a number of recent developments in microbiology – including biofilm formation, chemotaxis, quorum sensing and gene transfer – that highlight microbial capacities for cooperation and communication and break down conventional thinking that microbes are solely or primarily single-celled organisms. These insights also bring new perspectives to the levels of selection debate, as well as to discussions of the evolution and nature of multicellularity, and to neo-Darwinian understandings of evolutionary mechanisms. We show how these revisions lead to further complications for microbial classification and the philosophies of systematics and biodiversity. Incorporating microbial insights into the philosophy of biology will challenge many of its assumptions, but also give greater scope and depth to its investigations

    Search for Bs0B^{0}_{s} oscillations using inclusive lepton events

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    A search for Bs oscillations is performed using a sample of semileptonic b-hadron decays collected by the ALEPH experiment during 1991-1995. Compared to previous inclusive lepton analyses, the prop er time resolution and b-flavour mistag rate are significantly improved. Additional sensitivity to Bs mixing is obtained by identifying subsamples of events having a Bs purity which is higher than the average for the whole data sample. Unbinned maximum likelihood amplitude fits are performed to derive a lower limit of Dms>9.5 ps-1 at 95% CL. Combining with the ALEPH Ds based analyses yields Dms>9.6 ps-1 at 95% CL.A search for B0s oscillations is performed using a sample of semileptonic b-hadron decays collected by the ALEPH experiment during 1991-1995. Compared to previous inclusive lepton analyses, the proper time resolution and b-flavour mistag rate are significantly improved. Additional sensitivity to B0s mixing is obtained by identifying subsamples of events having a B0s purity which is higher than the average for the whole data sample. Unbinned maximum likelihood amplitude fits are performed to derive a lower limit of Deltam_s>9.5ps^-1 at 95% CL. Combining with the ALEPH D-s based analyses yields Deltam_s>9.6ps^-1 at 95% CL

    Measurement of the tau lepton lifetime

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    Limit on Bs0B^0_s oscillation using a jet charge method

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    A lower limit is set on the B_{s}^{0} meson oscillation parameter \Delta m_{s} using data collected from 1991 to 1994 by the ALEPH detector. Events with a high transverse momentum lepton and a reconstructed secondary vertex are used. The high transverse momentum leptons are produced mainly by b hadron decays, and the sign of the lepton indicates the particle/antiparticle final state in decays of neutral B mesons. The initial state is determined by a jet charge technique using both sides of the event. A maximum likelihood method is used to set a lower limit of \, \Delta m_{s}. The 95\% confidence level lower limit on \Delta m_s ranges between 5.2 and 6.5(\hbar/c^{2})~ps^{-1} when the fraction of b quarks from Z^0 decays that form B_{s}^{0} mesons is varied from 8\% to 16\%. Assuming that the B_{s}^{0} fraction is 12\%, the lower limit would be \Delta m_{s} 6.1(\hbar/c^{2})~ps^{-1} at 95\% confidence level. For x_s = \Delta m_s \, \tau_{B_s}, this limit also gives x_s 8.8 using the B_{s}^{0} lifetime of \tau_{B_s} = 1.55 \pm 0.11~ps and shifting the central value of \tau_{B_s} down by 1\sigma

    Measurement of the Bs0^0_s lifetime and production rate with Ds−l+^-_s l^+ combinations in Z decays

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    The lifetime of the \bs meson is measured in approximately 3 million hadronic Z decays accumulated using the ALEPH detector at LEP from 1991 to 1994. Seven different \ds decay modes were reconstructed and combined with an opposite sign lepton as evidence of semileptonic \bs decays. Two hundred and eight \dsl candidates satisfy selection criteria designed to ensure precise proper time reconstruction and yield a measured \bs lifetime of \mbox{\result .} Using a larger, less constrained sample of events, the product branching ratio is measured to be \mbox{\pbrresult
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