1,721,127 research outputs found

    Replication Data for: "Reversible NMR Hyperpolarization of 15N in Unmodified Amino Acids Unravelled at High Magnetic Field"

    No full text
    Replication Data for: "Reversible NMR Hyperpolarization of 15N in Unmodified Amino Acids Unravelled at High Magnetic Field

    Replication Data for: ‘Magneto-Hydrodynamic Mixing: a New Technique for Preparing Carbomer Hydrogels’

    No full text
    Replication data for Figures 3, 4 and S3 of the related publication

    3D Correlation of Solid-State NMR Parameters for Alumina - 3D interactive chart

    No full text
    Synthetic transition aluminas (χ, κ, θ, γ, δ, η, ρ) exhibit unique adsorptive and catalytic properties leading to numerous practical applications. Generated by thermal transformation of aluminium (oxy)hydroxides, structural differences between them arise from the variability of aluminium coordination numbers and degree of dehydroxylation. Unequivocal identification of these phases using X-ray diffraction has proven to be very difficult. Quadrupolar interactions of 27Al nuclei, highly sensitive to each site symmetry, render advanced 27Al solid-state NMR a unique spectroscopic tool to fingerprint and identify the different phases. In this paper, 27Al NMR spectroscopic data on alumina reported in literature are collected in a comprehensive library. Based on this dataset, a new 3D correlative method of NMR parameters is presented, enabling fingerprinting and identification of such phases. Providing a gold standard from crystalline samples, this approach demonstrates that any sort of crystalline, ill crystallized or amorphous, mixed periodic or aperiodically ordered transition alumina can now be assessed beyond the current limitations of characterisation. Adopting the presented approach as a standard characterisation of alumina samples, will readily reveal NMR parameter – structure – property relations suitable to develop new or improved applications of alumina

    3D Correlation of Solid-State NMR Parameters for Alumina - 3D interactive chart

    No full text
    Synthetic transition aluminas (χ, κ, θ, γ, δ, η, ρ) exhibit unique adsorptive and catalytic properties leading to numerous practical applications. Generated by thermal transformation of aluminium (oxy)hydroxides, structural differences between them arise from the variability of aluminium coordination numbers and degree of dehydroxylation. Unequivocal identification of these phases using X-ray diffraction has proven to be very difficult. Quadrupolar interactions of 27Al nuclei, highly sensitive to each site symmetry, render advanced 27Al solid-state NMR a unique spectroscopic tool to fingerprint and identify the different phases. In this paper, 27Al NMR spectroscopic data on alumina reported in literature are collected in a comprehensive library. Based on this dataset, a new 3D correlative method of NMR parameters is presented, enabling fingerprinting and identification of such phases. Providing a gold standard from crystalline samples, this approach demonstrates that any sort of crystalline, ill crystallized or amorphous, mixed periodic or aperiodically ordered transition alumina can now be assessed beyond the current limitations of characterisation. Adopting the presented approach as a standard characterisation of alumina samples, will readily reveal NMR parameter – structure – property relations suitable to develop new or improved applications of alumina

    Replication Data for: 'Techno-economic analysis of residential-scale seasonal energy storage using hydrogen'

    No full text
    Replication data for 'Techno-economic analysis of residential-scale seasonal energy storage using hydrogen

    Replication Data for: Isothermal (22 °C) evolution of the 1H MAS NMR spectrum and dielectric shift of water in Posisil foam with MAS frequency

    No full text
    Isothermal (22 °C) evolution of the 1H NMR spectrum of water in Posisil foam with MAS frequency (15 kHz = ± 4.5 MPa intrusion pressure). https://doi.org/10.1039/C9CS00545E - Figure 9 Isothermal (22 °C) evolution of the left spinning sideband, frequency offset corrected https://doi.org/10.1039/C9CS00545E - Figure 9 (Inset (top) Isothermal (22 °C) evolution of the dielectric shift (compared to a static sample). https://doi.org/10.1039/C9CS00545E - Figure 9 (Inset (bottom) </UL
    corecore