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GHG network analysis FMCG
(2013)
Novel hybrid admixtures for construction applications were prepared by layer-by-layer deposition technique. Colloidal core templates consisting of styrene/n-butylacrylate latex particles were coated with multilayers of superplasticizers commonly used in concrete. This way, core-shell particles possessing both dispersing and film-forming properties were achieved. Incorporation of the latex@dispersant hybrid additive into a cement paste results in a slow release of the superplasticizer as a result of gradual shell disintegration which instigates prolonged plastification (long ”slump life”) of the cement slurry. Once the shell has been dissolved, latex particles are released into the pore solution and can coalesce into a polymer film which improves the mechanical properties of the hardened cement. Characterization of the templates and novel additives was performed by means of zeta potential measurement, dynamic light scattering and electron microscopy. Our method allows to synthesize multifunctional additives with time-controlled release effect.
Novel microcapsules were prepared from colloidal core–shell particles by acid dissolution of the organic core. Weakly crosslinked, monodisperse and spherical melamine-formaldehyde polycondensate particles (diameter ∼ 1 μm) were synthesized as core template and coated with multilayers of an anionic polyelectrolyte via layer-by-layer deposition technique. As polyelectrolytes, an anionic naphthalenesulfonate formaldehyde polycondensate that is a common concrete superplasticizer and thus industrially available, and cationic poly(allylamine hydrochloride) were used. Core removal was achieved by soaking the core–shell particles in aqueous hydrochloric acid at pH 1.6, resulting in hollow microcapsules consisting of the polyelectrolytes. Characterization of the template, the core–shell particles, and the microcapsules plus tracking of the layer-by-layer polyelectrolyte deposition was performed by means of zeta potential measurement and scanning electron microscopy. The microcapsules might be useful as microcontainers for cement additives.
Several methods were employed to study the time dependent film formation of a self synthesized anionic latex dispersion in water and cement pore solution. First, a model carboxylated styrene/n-butyl acrylate latex dispersion possessing a minimum film forming temperature (MFFT) of 18 °C and a glass transition temperature (Tg) of 30 °C was synthesized via emulsion polymerization. Next, its film forming behaviour was studied at 40 °C, using an ESEM instrument. The analysis revealed that upon removal of water, film formation occurs as a result of particle packing, particle deformation and finally particle coalescence. Film formation is significantly hindered in synthetic cement pore solution. This effect can be ascribed to adsorption of Ca2+ ions onto the surface of the anionic latex particles and to interfacial secondary phases. This layer of adsorbed Ca2+ ions hinders interdiffusion of the macromolecules and subsequent film formation of the latex polymer.
People can exert control over the contents of their memory and can intentionally forget information when cued to do so. The present study examined such intentional forgetting in older adults using the listwise directed forgetting (DF) task. We replicated prior work by finding intact forgetting in young-old adults (up to 75 years). Extending the prior work, we additionally found forgetting to decline gradually with individuals' age and to be inefficient in old-old adults (above 75 years). The results indicate that listwise DF is a late-declining capability, suggesting a deficit in very old adults' episodic memory control.
The spectroscopy of molecules doped into superfluid helium droplets provides information on both, the dopant molecule and the helium environment. Electronic spectra of 9,10-dichloroanthracene in helium droplets are presented and compared with corresponding gas phase spectra to unravel the influence of the helium environment. The combined investigation of fluorescence excitation and dispersed emission provides information on dynamic processes in addition to energetic conditions. For vibronic states, the helium induced decay channels dominate over all intramolecular channels that contribute to the gas phase behavior. In addition to the triplet splitting caused by the Cl isotopes, a fine structure resolved for all transitions in the fluorescence excitation spectrum was found, which is the signature of microsolvation of this compound in helium droplets. This fine structure is identified as a single pure molecular transition accompanied by a sharply structured phonon wing. The corresponding fine structure measured for bare anthracene shows remarkable differences.
We show that a 450 fs nonresonant, moderately intense, linearly polarized laser pulse can induce field-free molecular axis alignment of methyliodide (CH3I) molecules dissolved in a helium nanodroplet. Time-resolved measurements reveal rotational dynamics much slower than that of isolated molecules and absence of the sharp transient alignment recurrences characteristic of gas phase molecules. Our results presage a range of new opportunities for exploring both molecular dynamics in a dissipative environment and the properties of He nanodroplets.
A moderately intense, nonresonant, linearly polarized nanosecond laser pulse is used to induce one-dimensional (1D) adiabatic alignment of 1,4 diiodobenzene (C6H4I2), iodobenzene (C6H5I), and methyliodide (CH3I) molecules dissolved in helium nanodroplets. The alignment sharpens as the laser intensity is increased, similar to the behavior in gas phase. For diiodobenzene the highest degree of alignment, ⟨cos2θ2D⟩=0.90, is essentially identical to the value obtained for isolated molecules in a supersonic beam, whereas the highest degrees of alignment for iodobenzene and for methyliodide in helium droplets fall below the values obtained for isolated molecules. We believe this is due to the deviation from axial recoil in the Coulomb explosion process that probes the alignment of the molecules in the He droplets.
After almost two decades of high resolution molecular spectroscopy in superfluid helium droplets, the understanding of microsolvation is still the subject of intense experimental and theoretical research. According to the published spectroscopic work including microwave, infrared, and electronic spectroscopy, the latter appears to be particularly promising to study microsolvation because of the appearance of pure molecular transitions and spectrally separated phonon wings. Instead of studying the very details of the influence of the helium environment for one particular dopant molecule as previously done for phthalocyanine, the present study compares electronic spectra of a series of non-polar porphyrin derivatives when doped into helium droplets consisting of 104–105 helium atoms. Thereby, we focus on the helium-induced fine structure, as revealed most clearly at the corresponding electronic origin. The interpretation and the assignment of particular features obtained in the fluorescence excitation spectra are based on additional investigations of dispersed emission spectra and of the saturation behavior. Besides many dopant-specific results, the experimental study provides strong evidence for a particular triple peak feature representing the characteristic signature of helium solvation for all seven related dopant species.