The preparation and characterisation of a novel, water-proof, irreversible, reusable, UV-activated, O(2) sensitive, smart plastic film is described. A pigment, consisting of a redox dye, methylene blue (MB), and a sacrificial electron donor, DL-threitol, coated onto an inorganic support with semiconductor functionality, TiO(2), has been extruded in low-density polyethylene (LDPE). The blue-coloured indicator is readily photobleached in <90 s using UVA light (4 mW cm(-2)), whereby MB is converted to its colourless, leuco form, leuco-methylene blue (LMB). This form persists in the absence of oxygen, but is re-oxidised to MB in ~2.5 days in air under ambient conditions (∼21 °C, ~65% RH) within the O(2) smart plastic film. The rate of recovery is linearly dependent upon the ambient level of O(2). At the lower temperature of 5 °C, the kinetics of the photobleaching activation step is largely unchanged, whereas that of recovery is markedly reduced to t(1/2) = 36 h at 5 °C (cf. 9 h at 21 °C); the activation energy for the recovery step was calculated as 28 kJ mol(-1). The O(2)-sensitive recovery step was found to be moderately dependent upon humidity at 21 °C, but not significantly dependent upon humidity at 5 °C. The possible application of this type of indicator in food packaging is illustrated and discussed briefly.
An experimental search for crystalline forms of creatine including a variable temperature X-ray powder diffraction study has produced three polymorphs and a formic acid solvate. The crystal structures of creatine forms I and II were determined from X-ray powder diffraction data plus the creatine formic acid (1 : 1) solvate structure was obtained by single crystal X-ray diffraction methods. Evidence of a third poly-morphic form of creatine obtained by rapid desolvation of creatine monohydrate is also presented. The results highlight the role of automated parallel crystallisation, slurry experiments and VT-XRPD as powerful techniques for effective physical form screening. They also highlight the importance of various complementary analytical techniques in structural characterisation and in achieving better understanding of the relationship between various solid-state forms. The structural relationships between various solid-state forms of creatine using the XPac method provided a rationale for the different relative stabilities of forms I and II of creatine with respect to the monohydrate form.
When solving the crystal structure of complex molecules from powder data, accurately locating the global minimum can be challenging, particularly where the number of internal degrees of freedom is large. The program Mogul provides a convenient means to access typical torsion angle ranges for fragments related to the molecule of interest. The impact that the application of modal torsion angle constraints has on the structure determination process of two structure solution attempts using DASH is presented. Once solved, accurate refinement of a molecular structure against powder data can also present challenges. Geometry optimisation using density functional theory in CASTEP is shown to be an effective means to locate hydrogen atom positions reliably and return a more accurate description of molecular conformation and intermolecular interactions than global optimisation and Rietveld refinement alone
The Prigogine principle of corresponding states for chain-molecule liquids is tested using published density, thermal expansion coefficient and isothermal compressibility data for the n-alkane series from methane to polymethylene. The principle is well obeyed allowing reduction parameters P*, V* and T* to be determined. The equation-of-state data for the pure liquids and the corresponding states theory applied to their mixtures permit the accurate prediction of excess volumes and their temperature and pressure dependence. Theoretical equations of state based upon the cell partition function (including the new Flory theory) show systematic errors. Analyses of experimental data using these theories produce, as artefacts, a variation of the reduction parameters with T, and an important decrease of P* with decreasing chain index. The present analysis shows P* to be constant to 3rl % from polymethylene to butane indicating that the terminal methyl groups and the interior methylene groups are similar in intermolecular contact energies. Without end-effects, the cell model theories predict an incorrect negative sign for H E of n-alkane mixtures at ordinary temperatures.
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