HERWIG 6.5 Release Note

A new release of the Monte Carlo program HERWIG (version 6.5) is now available. The main new features are: support for the Les Houches interface to matrix element generators; additional SM and MSSM Higgs processes in lepton collisions; additional matrix elements for the spin correlation algorithm; a new version of the ISAWIG interface; interface to the MC@NLO program for heavy quark, Higgs and vector boson production in hadron collisions. boson pair production in hadron collisions. This is planned to be the last major release of Fortran HERWIG. Future developments will be implemented in a new C++ event generator, HERWIG++

Quantitative study of hydration of C3S and C2S by thermal analysis. Evolution and composition of C-S-H gels formed

This research is part of a European project (namely, CODICE project), main objective of which is modelling, at a multi-scale, the evolution of the mechanical performance of non-degraded and degraded cementitious matrices. For that, a series of experiments were planned with pure synthetic tri-calcium silicate (C3S) and bi-calcium silicate (C2S) (main components of the Portland cement clinker) to obtain different calcium–silicate–hydrate (C–S–H) gel structures during their hydration. The characterization of those C–S–H gels and matrices will provide experimental parameters for the validation of the multi-scale modelling scheme proposed. In this article, a quantitative method, based on thermal analyses, has been used for the determination of the chemical composition of the C–S–H gel together with the degree of hydration and quantitative evolution of all the components of the pastes. Besides, the microstructure and type of silicate tetrahedron and mean chain length (MCL) were studied by scanning electron microscopy (SEM) and 29Si magic-angle-spinning (MAS) NMR, respectively. The main results showed that the chemical compositions for the C–S–H gels have a CaO/SiO2 M ratio almost constant of 1.7 for both C3S and C2S compounds. Small differences were found in the gel water content: the H2O/SiO2 M ratio ranged from 2.9 ± 0.2 to 2.6 ± 0.2 for the C3S (decrease) and from 2.4 ± 0.2 to 3.2 ± 0.2 for the C2S (increase). The MCL values of the C–S–H gels, determined from 29Si MAS NMR, were 3.5 and 4 silicate tetrahedron, for the hydrated C3S and C2S, respectively, remaining almost constant at all hydration periods

Clarification of possible ordered distributions of trivalent cations in layered double hydroxides and an explanation for the observed variation in the lower solid-solution limit.

The sequence of hexagonal ordered distributions of trivalent cations that are possible in the octahedral layer of layered double hydroxides is clarified, including the link between the composition and the supercell a parameter. A plausible explanation is provided for the observed variation in the lower solid-solution limit

Psychometric analysis of the scale for the predisposition to the occurrence of adverse events in nursing care provided in ICUS

OBJECTIVE: to present the result of the validity and reliability studies concerning the Scale for the Predisposition to the Occurrence of Adverse Events (EPEA). METHOD: construct validity was based on Principal Components Analysis. RESULTS: reliability verified through Cronbach's alpha indicated good reliability (structure α=0.80; process α=0.92). CONCLUSION: based on its psychometric indicators, the EPEA can be considered a valid measure to assess the attitudes of nurses in relation to factors that potentially lead to the occurrence of adverse events in ICUs

Composition and structure of an 18-year-old 5M KOH-activated ground granulated blast-furnace slag paste

The main hydration products were C-A-S-H(I), present in both inner (Ip) and outer product (Op), and a Mg-Al layered double hydroxide (LDH), present only in the Ip. The composition of C-A-S-H(I) was the same in Op and Ip. Reduced scatter in the data with age suggests a tendency towards compositional homogeneity. The mean length of the aluminosilicate anions in the C-A-S-H(I) increased with age. The layer spacings of the C-A-S-H(I) and Mg-Al LDH had not changed significantly with age. The Mg/Al ratio of the LDH was about 2.6 and had not changed between 1 and 18 years

Are attitudes towards medication adherence associated with medication adherence behaviours among patients with psychosis? A systematic review and meta analysis

Background Studies have shown patient attitudes to be an important predictor for health related behaviours including medication adherence. It is less clear whether patient attitudes are also associated with medication adherence among patients with psychoses. Method We conducted a systematic review and meta analysis of the data of studies that tested the association of attitude measures with medication adherence among patients with psychoses. 14 studies conducted between 1980 and 2010 were included. Results Results show a small to moderate mean weighted effect size (r + = 0.25 and 0.26 for Pearson and Spearman correlations, respectively). Conclusions Theory based interventions that target potentially modifiable attitude components are needed to assess the relationship between positive patient attitudes and adherence behaviours among patients with psychoses

The mechanism of supplementary cementitious materials enhancing the water resistance of magnesium oxychloride cement (MOC): A comparison between pulverized fuel ash and incinerated sewage sludge ash

Magnesium oxychloride cement (MOC) pastes incorporating supplementary cementitious materials (SCMs) including pulverized fuel ash (PFA) and incinerated sewage sludge ash (ISSA) were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) with energy dispersive X-ray spectrometry (EDX). The result showed that the mechanism of PFA and ISSA in improving the water resistance of MOC paste is similar, even though the molar ratios of the hydration product in the ISSA-incorporated paste and the PFA-incorporated paste were different. The active phases in PFA or ISSA could react with MgO and produce an amorphous phase (amorphous magnesium aluminosilicate gel), which was interspersed with Phase 5 and changed the morphology of Phase 5 to fibroid or lath-like phases. These fibroid or lath-like phases interlocked with each other and also connected with the amorphous phase in the matrix to form a stable compact structure. Therefore, the water resistance of MOC was improved. The ISSA-blended MOC paste had higher water resistance compared to the PFA-blended MOC, which may be due to the different chemical composition of amorphous phase and the dissolved phosphorus from ISSA

Hydration of dicalcium silicate and diffusion through neo-formed calcium-silicate-hydrates at weathered surfaces control the long-term leaching behaviour of basic oxygen furnace (BOF) steelmaking slag

Alkalinity generation and toxic trace metal (such as vanadium) leaching from basic oxygen furnace (BOF) steel slag particles must be properly understood and managed by pre-conditioning if beneficial reuse of slag is to be maximised. Water leaching under aerated conditions was investigated using fresh BOF slag at three different particle sizes (0.5–1.0, 2–5 and 10 × 10 × 20 mm blocks) and a 6-month pre-weathered block. There were several distinct leaching stages observed over time associated with different phases controlling the solution chemistry: (1) free-lime (CaO) dissolution (days 0–2); (2) dicalcium silicate (Ca₂SiO₄) dissolution (days 2–14) and (3) Ca–Si–H and CaCO₃ formation and subsequent dissolution (days 14–73). Experiments with the smallest size fraction resulted in the highest Ca, Si and V concentrations, highlighting the role of surface area in controlling initial leaching. After ~2 weeks, the solution Ca/Si ratio (0.7–0.9) evolved to equal those found within a Ca–Si–H phase that replaced dicalcium silicate and free-lime phases in a 30- to 150-μm altered surface region. V release was a two-stage process; initially, V was released by dicalcium silicate dissolution, but V also isomorphically substituted for Si into the neo-formed Ca–Si–H in the alteration zone. Therefore, on longer timescales, the release of V to solution was primarily controlled by considerably slower Ca–Si–H dissolution rates, which decreased the rate of V release by an order of magnitude. Overall, the results indicate that the BOF slag leaching mechanism evolves from a situation initially dominated by rapid hydration and dissolution of primary dicalcium silicate/free-lime phases, to a slow diffusion limited process controlled by the solubility of secondary Ca–Si–H and CaCO₃ phases that replace and cover more reactive primary slag phases at particle surfaces