What Motivates Staff to Work at a Therapeutic School for Children Identified as Having Social, Emotional and Behavioural Difficulties?

Those who work at schools with children identified as having social, emotional and behavioural difficulties (SEBD), work in considerably challenging, stressful and undesirable environments (Shuttleworth, 2005). Taking this into consideration, this study focuses on staff motivation, in an attempt to pinpoint what motivates individuals to pursue and commit to a career in this field of work. Staff members working with children identified as having SEBD at a therapeutic primary school in the UK were interviewed (N = 7). Semi-structured interviews were prepared and carried out inside the school premises in a private space. Interviews were recorded using an audio recorder and were analysed using thematic analysis (Braun & Clarke, 2006). Self-determination theory (Ryan & Deci, 2000) was applied to the data and referred to as a framework. Five key themes were developed from the data, three of the key themes were deemed to be most relevant to the research question: ‘What motivates staff to work at a therapeutic school for children identified as having emotional and behavioural difficulties?’ These were: Emotional connection: Occasions when participants spoke of feeling deeply connected to others. This connection was either with children through relatedness, or with colleagues (team spirit). A sense of feeling good: This was summarised as pride, enjoyment, appreciation, a sense of feeling right/suited, feeling valued, and even ‘the challenge’ and ‘hard work’. Responsibility: Participants felt driven by a sense of responsibility, for example comparisons were made to being like parent-figures to the children. These three themes were considered to be the key forms of motivation identified from this particular sample of staff members

Accurate simulation estimates of phase behaviour in ternary mixtures with prescribed composition

This paper describes an isobaric semi-grand canonical ensemble Monte Carlo scheme for the accurate study of phase behaviour in ternary fluid mixtures under the experimentally relevant conditions of prescribed pressure, temperature and overall composition. It is shown how to tune the relative chemical potentials of the individual components to target some requisite overall composition and how, in regions of phase coexistence, to extract accurate estimates for the compositions and phase fractions of individual coexisting phases. The method is illustrated by tracking a path through the composition space of a model ternary Lennard-Jones mixture.Comment: 6 pages, 3 figure

Effects of Confinement on Critical Adsorption: Absence of Critical Depletion for Fluids in Slit Pores

The adsorption of a near-critical fluid confined in a slit pore is investigated by means of density functional theory and by Monte Carlo simulation for a Lennard-Jones fluid. Our work was stimulated by recent experiments for SF_6 adsorbed in a mesoporous glass which showed the striking phenomenon of critical depletion, i.e. the adsorption excess "Gamma" first increases but then decreases very rapidly to negative values as the bulk critical temperature T_c is approached from above along near-critical isochores. By contrast, our density functional and simulation results, for a range of strongly attractive wall-fluid potentials, show Gamma monotonically increasing and eventually saturating as the temperature is lowered towards T_c along both the critical (rho=rho_c) and sub-critical isochores (rho<\rho_c). Such behaviour results from the increasingly slow decay of the density profile away from the walls, into the middle of the slit, as T->T_c. For rho < rho_c we find that in the fluid the effective bulk field, which is negative and which favours desorption, is insufficient to dominate the effects of the surface fields which favour adsorption. We compare this situation with earlier results for the lattice gas model with a constant (negative) bulk field where critical depletion was found. Qualitatively different behaviour of the density profiles and adsorption is found in simulations for intermediate and weakly attractive wall-fluid potentials but in no case do we observe the critical depletion found in experiments. We conclude that the latter cannot be accounted for by a single pore model.Comment: 21 pages Revtex. Submitted to Phys. Rev.

Effects of weak surface fields on the density profiles and adsorption of a confined fluid near bulk criticality

The density profile and Gibbs adsorption of a near-critical fluid confined between two identical planar walls is studied by means of Monte Carlo simulation and by density functional theory for a Lennard-Jones fluid. By reducing the strength of wall-fluid interactions relative to fluid-fluid interactions we observe a crossover from behaviour characteristic of the normal surface universality class, strong critical adsorption, to behaviour characteristic of a 'neutral' wall. The crossover is reminiscent of that which occurs near the ordinary surface transition in Ising films subject to vanishing surface fields. For the 'neutral' wall the density profile, away from the walls, is almost constant throughout the slit capillary and gives rise to an adsorption that is constant along the critical isochore. The same 'neutral' wall yields a line of capillary coexistence that is almost identical to the bulk coexistence line. In the crossover regime we observe features in the density profile similar to those found in the magnetisation profile of the critical Ising film subject to weak surface fields, namely two smooth maxima, located away from the walls, which merge into a single maximum at midpoint as the strength of the wall-fluid interaction is reduced or as the distance between walls is decreased. We discuss similarities and differences between the surface critical behaviour of fluids and of Ising magnets.Comment: 34 pages, 10 figures, submitted to the Journ. Chem. Phy

Enthalpies of formation of lanthanide oxyapatite phases

A family of lanthanide silicates adopts an oxyapatite-like structure with structural formula Ln9.33∎0.67(SiO4)6O2 (Ln 4 La, Sm, Nd, Gd, ∎ = vacancy). The enthalpies of solution, DHS, for these materials and their corresponding binary oxides were determined by high-temperature oxide melt solution calorimetry using molten 2PbO·B2O3 at 1078 K. These data were used to complete thermodynamic cycles to calculate enthalpies of formation from the oxides, ΔHs f-oxides (kJ/mol): La9.33∎0.67(SiO4)6O2 = −776.3 ± 17.9, Nd9.33∎0.67(SiO4)6O2 = −760.4 ± 31.9, Sm9.33∎0.67(SiO4)6O2 = −590.3 ± 18.6, and Gd9.33∎0.67(SiO4)6O2 = −446.9 ± 21.9. Reference data were used to calculate the standard enthalpies of formation from the elements, ΔH0 f (kJ/mol): La9.33∎0.67(SiO4)6O2 = −14611.0 ± 19.4, Nd9.33∎0.67(SiO4)6O2 = −14661.5 ± 32.2, Sm9.33∎0.67(SiO4)6O2 = −14561.7 ± 20.8, and Gd9.33∎0.67(SiO4)6O2 = −14402.7 ± 28.2. The formation enthalpies become more endothermic as the ionic radius of the lanthanide ion decreases

Freezing line of the Lennard-Jones fluid: a Phase Switch Monte Carlo study

We report a Phase Switch Monte Carlo (PSMC) method study of the freezing line of the Lennard-Jones (LJ) fluid. Our work generalizes to soft potentials the original application of the method to hard sphere freezing, and builds on a previous PSMC study of the LJ system by Errington (J. Chem. Phys. {\bf 120}, 3130 (2004)). The latter work is extended by tracing a large section of the Lennard-Jones freezing curve, the results for which we compare to a previous Gibbs-Duhem integration study. Additionally we provide new background regarding the statistical mechanical basis of the PSMC method and extensive implementation details.Comment: 18 pages, 6 figure

Metastable liquid-liquid coexistence and density anomalies in a core-softened fluid

Linearly-sloped or `ramp' potentials belong to a class of core-softened models which possess a liquid-liquid critical point (LLCP) in addition to the usual liquid-gas critical point. Furthermore they exhibit thermodynamic anomalies in the density and compressibility, the nature of which may be akin to those occurring in water. Previous simulation studies of ramp potentials have focused on just one functional form, for which the LLCP is thermodynamically stable. In this work we construct a series of ramp potentials, which interpolate between this previously studied form and a ramp-based approximation to the Lennard-Jones (LJ) potential. By means of Monte Carlo simulation, we locate the LLCP, the first order high density liquid (HDL)-low density liquid (LDL) coexistence line, and the line of density maxima for a selection of potentials in the series. We observe that as the LJ limit is approached, the LLCP becomes metastable with respect to freezing into a hexagonal close packed crystalline solid. The qualitative nature of the phase behaviour in this regime shows a remarkable resemblance to that seen in simulation studies of accurate water models. Specifically, the density of the liquid phase exceeds that of the solid; the gradient of the metastable LDL-HDL line is negative in the pressure (p)-temperature (T) plane; while the line of density maxima in the p-T plane has a shape similar to that seen in water and extends well into the {\em stable} liquid region of the phase diagram. As such, our results lend weight to the `second critical point' hypothesis as an explanation for the anomalous behaviour of water.Comment: 7 pages, 8 figure