Hydrothermal synthesis of layered zirconium phosphates and their intercalation properties.

Layered inorganic materials are widely used as fillers in nanocomposites due to their unique properties such as mechanical performance, thermal properties, flame resistance, barrier properties, corrosion resistance, catalytic activity, and multifunctionality. Among them, layered α-zirconium phosphate (α-ZrP: Zr(HPO4)2H2O) is one of the representative inorganic materials and unique properties with P-O-H groups that can exchange inorganic and organic cations and intercalate basic molecules. This paper deals with the use of this compound as an adsorbent for heavy metal cations in wastewater. Samples were prepared by hydrothermal treatment at various Zr/P ratio, water amounts, and temperatures. Furthermore, an attempt was made to widen the interlayer distance of the sample using n-butylamine. The α- zirconium phosphate prepared at 160°C for 20 h with Zr/P = 1/2 adsorbed the most amount of metal ions. Furthermore, interlayer amine modification was effective. Then, the behaviour of the adsorption process was observed by varying the time of adsorption from 1 h to 50 h, in order to clarify the change in adsorption of the samples over time.

Synthesis of Cobalt-Substituted Manganese Phosphate Purple Pigments.

Some manganese phosphates are known as violet pigments. In this study, pigments in which manganese was partially replaced with cobalt and aluminum was replaced with lanthanum and cerium were synthesized with a heating method to obtain pigments with a more reddish color. The obtained samples were evaluated in terms of chemical composition, hue, acid and base resistances, and hiding power. Among the samples examined, the samples obtained in the Co/Mn/La/P system were the most vivid. The brighter and redder samples were obtained by prolonged heating. Furthermore, prolonged heating improved the acid and base resistance of the samples. Finally, the substitution of manganese for cobalt improved the hiding power.

Selective preparation of samarium phosphates from transition metal mixed solution by two-step precipitation.

Samarium-cobalt alloys are used as materials for powerful magnets with relatively high Curie temperatures. Samarium is a valuable and expensive material because it is one of a group of rare earth elements. In order to utilize this rare earth resource in a sustainable society, it is necessary to recover, reuse, and recycle rare earth elements. With this in mind, a new process for recovering neodymium phosphate from neodymium-iron mixed aqueous solutions has recently been reported, avoiding the difficulties reported with conventional methods. Given that rare earth phosphates are a major component of rare earth ores, this new process was proposed to recover them as phosphates. In this method, neodymium phosphate was selectively precipitated from a neodymium-iron mixture in a two-step process with an adjusted pH value. In this study, we attempted to selectively precipitate samarium phosphate from a mixed solution of transition metals using this two-step precipitation method. The advantage of this method is that the samarium compound can be separated from other metal salts without the use of high temperatures or special equipment. Optimal conditions were determined by evaluating the precipitates by molar ratio, color hue, UV-visible reflectance spectra, X-ray diffraction, and infrared spectroscopy of the precipitates obtained. In Step 1, the pH was adjusted using sodium hydroxide to remove cobalt, iron, and copper hydroxides other than samarium. In Step 2, after adding phosphoric acid, the pH was adjusted so that a precipitate of samarium phosphate was formed.

Bismuth titanate-based UV filters embedded mesoporous silica nanoparticles: Role of bismuth concentration in the self-sealing process.

The development of new safe inorganic UV filters to effectively protect the skin from ultraviolet (UV) radiation effects is an emerging issue. Bismuth titanate-based UV filters embedded into mesoporous silica nanoparticles (MSN) represent a new class of inorganic sunscreens, with excellent UVA and UVB shielding properties. In addition, the presence of bismuth ions promotes a self-sealing process, allowing (i) the entrapment of the active phases in the deepest core of the system and (ii) the formation of an external glassy silica layer with a consequent suppression of the photocatalytic activity. In this work, aimed at studying in detail the self-sealing mechanism and accessing the role of bismuth ions in the formation of the system, a series of samples impregnated with a different amount of bismuth were investigated. The self-sealing process already occurs at the lowest content of bismuth and the mechanism is demonstrated to be triggered by the ability of Bi to work as a low-melting point agent for silica. Finally, a sunscreen formulation containing the new UV filter was prepared and the Sun Protection Factor (SPF), the pH and the viscosity were measured, demonstrating the potential of the proposed material for large-scale applications.

Preparation and fluorescence properties of crystalline gel rare earth phosphates.

An aqueous solution of sodium dihydrogen phosphate was mixed with a aqueous solution of lanthanum nitrate and stirred for 24 h, and the pH was adjusted to 11 using ammonia. The obtained phosphates were analyzed using X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetry-differential thermal analysis, and scanning electron microscopy. The lanthanum phosphate gel was obtained with a large amount of water. The fluorescence of the gels was investigated by substituting a part of the lanthanum cations with cerium, terbium, and europium cations. UV-vis reflectance and fluorescence spectra of these substituted materials were obtained and analyzed. Rrare-earth phosphate gels with large amounts of water exhibited bluish purple, green, and red fluorescence when cation ratios of La/Ce = 70/30, La/Ce/Tb = 55/30/15, and La/Eu = 95/5 were used, respectively.

Preparation of titanium phosphates with additives in hydrothermal process and their powder properties for cosmetics.

In this study, titanium phosphates were prepared from titanium chloride and phosphoric acid, sodium pyrophosphate and sodium triphosphate solutions with water retention compounds in hydrothermal process as a novel white pigment for cosmetics. Their chemical composition, powder properties, photo catalytic activity, water retention and smoothness were studied. The addition of glycerin in the preparation from sodium pyrophosphate has the useful method to obtain homogenized spherical particles of titanium phosphate pigments for the cosmetics. These titanium phosphates had less photo catalytic activity to protect the sebum on the skin.