1,229 research outputs found

    Stokes settling and particle-laden plumes: implications for deep-sea mining and volcanic eruption plumes

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    Turbulent buoyant plumes moving through density stratified environments transport large volumes of fluid vertically. Eventually, the fluid reaches its neutral buoyancy level at which it intrudes into the environment. For single-phase plume, the well known theory of Morton, Taylor and Turner [1] describes the height of the intrusion with great accuracy. However, in multiphase plumes, such as descending particle plumes formed from the surface vessel during deep- sea mining operations, or ascending volcanic plumes, consisting of hot gas and dense ash particles, the sedimentation of particles can change the buoyancy of the fluid very significantly. Even if the plume speed far exceeds the sedimentation speed, the ultimate intrusion height of the fluid may be significantly affected by particle sedimentation. We explore this process, illustrating the phenomena with a series of analogue experiments and some simple modelling, and we discuss the applications in helping to quantify some environmental impacts of deep-sea mining and in helping to assess the eruption conditions leading to the formation of large laterally spreading ash clouds in the atmosphere

    Thermodynamic stability of alkali metal/zinc double-cation borohydrides at low temperatures

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    We study the thermodynamic stability at low temperatures of a series of alkali metal/zinc double-cation borohydrides, including LiZn(BH4_4)3_3, LiZn2_2(BH4_4)5_5, NaZn(BH4_4)3_3, NaZn2_2(BH4_4)5_5, KZn(BH4_4)3_3, and KZn2_2(BH4_4)5_5. While LiZn2_2(BH4_4)5_5, NaZn(BH4_4)3_3, NaZn2_2(BH4_4)5_5 and KZn(BH4_4)3_3 were recently synthesized, LiZn(BH4_4)3_3 and KZn2_2(BH4_4)5_5 are hypothetical compounds. Using the minima-hopping method, we discover two new lowest-energy structures for NaZn(BH4_4)3_3 and KZn2_2(BH4_4)5_5 which belong to the C2/cC2/c and P2P2 space groups, respectively. These structures are predicted to be both thermodynamically stable and dynamically stable, implying that their existence may be possible. On the other hand, the lowest-energy P1P1 structure of LiZn(BH4_4)3_3 is predicted to be unstable, suggesting a possible reason elucidating why this compound has not been experimentally identified. In exploring the low-energy structures of these compounds, we find that their energetic ordering is sensitive to the inclusion of the van der Waals interactions. We also find that a proper treatment of these interactions, e.g., as given by a non-local density functional such as vdW-DF2, is necessary to address the stability of the low-energy structures of these compounds.Comment: Final versio

    Platinum(IV)-azido monocarboxylato complexes are photocytotoxic under irradiation with visible light

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    Complexes trans,trans,trans-[Pt(N-3)(2)(OH)(OCOR)(py)(2)] where py = pyridine and where OCOR = succinate (1); 4-oxo-4-propoxybutanoate (2) and N-methylisatoate (3) have been synthesized by derivation of trans, trans,trans-[Pt(OH)(2)(N-3)(2)(py)(2)] (4) and characterised by NMR and EPR spectroscopy, ESI-MS and X-ray crystallography. Irradiation of 1-3 with green (517 nm) light initiated photoreduction to Pt(II) and release of the axial ligands at a 3-fold faster rate than for 4. TD-DFT calculations showed dissociative transitions at longer wavelengths for 1 compared to 4. Complexes 1 and 2 showed greater photocytotoxicity than 4 when irradiated with 420 nm light (A2780 cell line IC50 values: 2.7 and 3.7 mu M) and complex 2 was particularly active towards the cisplatin-resistant cell line A2780cis (IC50 3.7 mu M). Unlike 4, complexes 1-3 were phototoxic under green light irradiation (517 nm), with minimal toxicity in the dark. A pK(a)(H2O) of 5.13 for the free carboxylate group was determined for 1, corresponding to an overall negative charge during biological experiments, which crucially, did not appear to impede cellular accumulation and photocytotoxicity.NF thanks the Wellcome Trust (201406/Z/16/Z); Cancer Research UK (CR-UK) grant number C5255/A18085 through the Cancer Research UK Oxford Centre and the John Fell Fund for funding. NF thanks Profs. Stephen Faulkner for support. PJS and NF thank the EPSRC (for grant EP/P030572/1 and studentship for ES), PJS also thanks the ERC (grant 247450). L. S. performed this work under the Severo Ochoa Centres of Excellence Programme run by the Spanish State Research Agency, grant no. CEX2018-000867-S (DIPC). L. S. also thanks the Spanish Multi-MetDrugs network (RED2018-102471-T) for fruitful discussio
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