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This paper aims to introduce a novel approach to the fabrication of photoluminescent materials by coating rare earth aluminate luminescent materials on metallic substrates and a readily manufacturable light source with robust structure in the form of photoluminescent sphere (APS).

The clean and dried stainless steel sphere was sprayed with UH 2593, a white undercoat, the luminescent coating and the weather resistance coating in chronological order.

After adhered onto the stainless steel sphere, the peaks corresponding to the N-H stretching vibrations were changed. The intensity of free N-H stretching at 3,536 cm⁻¹ dramatically decreased and the peak of hydrogen-bonded N-H stretching of PU moved to lower wavenumbers. The red shift of the infrared bands of functional groups was attributed to the strengthened hydrogen bonding. The hydrogen bonding interactions between the stainless steel substrates and the polyurethane coating endowed the APS with excellent adhesive property and also promoted the evenly distribution of the photoluminescent particles in the polymer coating matrix.

This approach can be applicable in the fabrication of the photoluminescent materials. The APS can be used as signs and guiding post in remote areas without sufficient electricity supply and in the seas and rivers with complicated hydrological conditions.

This approach has provided a method to produce tough and durable luminescent signs for remote areas and dangerous seas and explained the functional mechanism of the combined application of metallic materials and non-metallic materials.

The purpose of this paper is to investigate three preparation processes and the photoluminescent (PL) properties of PbS/poly(p‐phenylene vinylene) (PPV) composite fibres.

By the combination of electrospinning technology, chemical vapour deposition and chemical liquid deposition, PbS/PPV composite nanofibres were prepared by three simple methods. The morphologies of the fibres and the PL properties were researched with the transmission electron microscopy (TEM) and the eclipse fluorescence spectrophotometer.

By different synthetic methods, the dispersion morphologies of PbS nanoparticles and the PL properties of their respective PbS/PPV composite fibres were different. Moreover, the effects of PbS nanoparticles on the luminescence quenching of the PPV were observed in all the synthesised PbS/PPV composite fibres, respectively.

The dispersion morphologies of PbS nanoparticles were not uniform enough.

A new method was used for preparing nanoparticles/polymer composite fibres.

The combination of electrospinning technology and chemical liquid deposition was used for the first time to fabricate the sulfide/polymer composite fibres. In addition, we hope that the results obtained here will provide some useful evidences for the interaction mechanism between IV‐VI group semiconductors and conjugated polymers, and the prepared composite fibres will have applications in the nano‐optoelectronic field.

This paper outlines the innovations in high functional and high performance fibres for applications in protective clothing, including fibres for flame and heat protection. It also describes some typical woven and non‐woven constructions for such applications. And presents the trends in producing smart textile materials, capable of interacting with human/environmental conditions.

NOW HERE is a funny sequence. We are told that actual pay is up above the inflation rate because so much overtime is being worked. If this was one of those stories where the audience is invited to cheer or groan alternately, we would say ‘Hurrah’!

This paper aims to systematically demonstrate a methodology to determine the relative and absolute encapsulation efficiencies (α_Re and α_Ab) for thermally- and chemically-robust inorganic pigments, typically like ZrSiO₄-based pigments, thereby enhancing their coloring performance.

The authors designed a route, surplus alkali-decomposition and subsequently strong-acid dissolution (SAD2) to completely decompose three classic zircon pigments (Pr–ZrSiO₄, Fe₂O₃@ZrSiO₄ and CdS@ZrSiO₄) into clear solutions and preferably used inductively coupled plasma-optical emission spectrometry (ICP-OES) to determine the concentrations of host elements and chromophores, thereby deriving the numeric data and interrelation of α_Re and α_Ab.

Zircon pigments can be thoroughly decomposed into some dissoluble zirconate–silicate resultants by SAD2 at a ratio of the fluxing agent to pigment over 6. ICP-OES is proved more suitable than some other quantification techniques in deriving the compositional concentrations, thereby the values of α_Re and α_Ab, and their transformation coefficient K_RA, which maintains stably within 0.8–0.9 in Fe₂O₃@ZrSiO₄ and CdS@ZrSiO₄ and is slightly reduced to 0.67–0.85 in Pr–ZrSiO₄.

The SAD2 method and encapsulation efficiencies are well applicable for both zircon pigments and the other pigmental or non-pigmental inhomogeneous systems in characterizing their accurate composition.

The authors herein first proposed strict definitions for the relative and absolute encapsulation efficiencies for inorganic pigments, developed a relatively stringent methodology to determine their accurate values and interrelation.