Environmentally Benign Solution‐Based Procedure for the Fabrication of Metal Oxide Coatings on Metallic Pigments

Aluminum pigments were coated with Fe₂O₃ and CuO by solution‐based thermal decomposition of the urea nitrate compounds hexakisureairon(III)nitrate and tetrakisureacopper(II)nitrate. The deposition process was optimized to obtain homogeneously coated aluminum pigments. The growth of the surface coatings was controlled by investigation with scanning electron microscopy, energy dispersive X‐ray spectroscopy and static light scattering as well as infrared, X‐ray diffraction and thermogravimetric analysis. The iron precursor showed an incomplete decomposition in solution, incorporating traces of urea molecules inside the coatings while the copper precursor showed complete dissociation accompanied by in situ formation of amine complexes. The amount of organic residues resulting from ligand fragments in the final oxide coatings could be reduced to 22 % for the iron oxide and 12 % for the copper oxide by further temperature treatment in solution (259 °C). Colorimetric investigations of the obtained pigments revealed an excellent hiding power, outperforming the pigments used in current state‐of‐the‐art formulations

Sandwich-Like Encapsulation of a Highly Luminescent Copper(I) Complex

A small molecular weight cationic copper(I) complex showing high luminescence quantum yield based on a thermally activated delayed fluorescence mechanism is immobilized between two 1 nm thin silicate layers. Partial ion exchange of the emitter into a synthetic layered silicate (fluorohectorite) yields an ordered heterostructure with two types of strictly alternating interlayers: a monolayer of the cationic emitter and a monolayer of hydrated Na+ cations. Osmotic swelling of the latter produces dispersions of double-stacks in which the emitter monolayer is encapsulated between two silicate layers. The electrostatic attraction of the emitter interlayer with the oppositely charged silicate layers exerts electrostatic pressure on the emitter. Compared to crystalline salt, rigid confinement for the encapsulated emitter provides improved thermal stability and increased emission quantum yield at ambient temperature. The suspension of delaminated, micrometer-sized double-stacks of 3.9 nm thickness allows for easy solution processing of low-cost optoelectronic devices, such as light-emitting electrochemical cells and organic light-emitting diodes

Environmentally benign solution‐based procedure for the fabrication of metal oxide coatings on metallic pigments

Aluminum pigments were coated with Fe₂O₃ and CuO by solution‐based thermal decomposition of the urea nitrate compounds hexakisureairon(III)nitrate and tetrakisureacopper(II)nitrate. The deposition process was optimized to obtain homogeneously coated aluminum pigments. The growth of the surface coatings was controlled by investigation with scanning electron microscopy, energy dispersive X‐ray spectroscopy and static light scattering as well as infrared, X‐ray diffraction and thermogravimetric analysis. The iron precursor showed an incomplete decomposition in solution, incorporating traces of urea molecules inside the coatings while the copper precursor showed complete dissociation accompanied by in situ formation of amine complexes. The amount of organic residues resulting from ligand fragments in the final oxide coatings could be reduced to 22 % for the iron oxide and 12 % for the copper oxide by further temperature treatment in solution (259 °C). Colorimetric investigations of the obtained pigments revealed an excellent hiding power, outperforming the pigments used in current state‐of‐the‐art formulations

The nature of laponite: pure hectorite or a mixture of different trioctahedral phases?

Summarization: A series of laponites and synthetic OH-and fluorinated hectorites prepared from hydrothermal and melting experiments at both industrial and laboratory scale were examined with XRD and FTIR (MIR and NIR) to determine their mineralogical composition and possible compositional heterogeneity. The end materials contained both Li-and Na-bearing phases. The industrial hydrothermal OH-smectites prepared at low temperatures consist of random mixed layer hectorite-stevensite-kerolite with about 40–50% hectorite layers, the remaining being stevensite and kerolite at roughly equal proportions. The FTIR spectra of these smectites contain, besides the main Mg3 OH stretching/overtone bands at 3695–3690 and 7225–7214 cm−1, respectively, additional OH overtone bands at ~3716 and 7265 cm−1 (hydrated state). These bands might be linked to Mg2 LiOH stretching modes. The melt-derived smectites are kerolite-free but still contain stevensite layers, although the preparation methods involved heating in the excess of 1000◦ C. In these smectites Li might be partitioned to both octahedral and interlayer sites. Subsequent annealing of the melt-derived Mg-Li smectites caused migration of the exchangeable Li to the vacant octahedral due to the Hofmann-Klemen effect and thus decrease of the layer charge, as was indicated by the νO-D method. Hydrothermal synthesis of Mg-Li smectites at high temperature (400◦ C) and pressure (1 kbar), yielded pure hectorite without stevensite or kerolite domains.Presented on: Mineral

Casein kinase 1 delta (CK1delta) interacts with the SNARE associated protein snapin

In this study we identified snapin as an interaction partner of the CK1 isoform delta (CK1delta) in the yeast two-hybrid system and localized the interacting domains of both proteins. The interaction of CK1delta with snapin was confirmed by co-immunoprecipitation. Snapin was phosphorylated by CK1delta in vitro. Both proteins localized in close proximity in the perinuclear region, wherein snapin was found to associate with membranes of the Golgi apparatus. The identification of snapin as a new substrate of CK1delta points towards a possible function for CK1delta in modulating snapin specific functions