Transformation of 1-D Chiral-chained Titanium Phosphate to 2-D Layer Structure Through a 1-D Zigzag Chain

The transformation of titanium phosphate from 1-D chiral- chain(JTP-A) to 2-D layer(TP-J1) has been carefully investigated. Through a hydrolysis-condensation self-assembly pathway, the crystals of TP-J1 can be obtained from the JTP-A phase under hydrothermal conditions. An intermediate material with zigzag chain during the transformation was observed by XRD characterization. A hypothesis of the transformation mechanism is also described in this article. It is noteworthy that ethylenediamine plays an important role in the transformation.

Zinc and Silver Salts-Containing Lamellar Titanium Phosphate: A Multifunctional Filler

Zinc and silver compounds have been studied because they have ultraviolet light barrier properties and bactericidal action, respectively. Materials with multifunctional characteristics have been sought to produce polymeric nanocomposites. In this work, the chemical modification of titanium phosphate (TiP) was carried out through a route with successive intercalations. TiP was synthesized and consecutively pre-expanded with ethylamine and pyromellitic acid. Then it was modified with zinc acetate and silver nitrate. The final product was characterized by Fourier transform infrared spectroscopy, differential scanning calorimetry, wide-angle X-ray diffractometry, field emission scanning electron microscopy coupled with energy dispersive X-ray spectroscopy and thermogravimetry. Infrared revealed dislocation and appearance of bands according to the intercalating agent. Inorganic salts interfered in the crystallization and melting processes of pyromellitic acid. Vanishing of the TiP hkl plane and variation and appearance of new crystallographic planes at low diffraction angles induced intercalation. SEM showed agglomerated structures. New thermal degradation events at higher temperatures endorsed the formation of zinc and silver carboxylate salts. We concluded that a new miscellaneous and multifunctional matter was achieved.

Preparation of titanium phosphate white pigments with titanium sulfate and their powder properties

Titanium oxide that has photocatalytic activity is used as white pigment for cosmetics.A certain degree of sebum on the skin is decomposed by the ultraviolet radiation in sunlight.In this work,as novel white pigment,titanium phosphates were synthesized with titanium sulfate and phosphoric acid for cosmetics.Their chemical composition,powder properties,photocatalytic activity,color phase,moisture retention,and smoothness were studied.These titanium phosphates had less photocatalytic activity to protect the sebum on the skin.Samples without heating and those heated at 100℃showed high reflectance in the range of visible light.Sample prepared in Ti/P=3/2 had higher moisture retention than samples prepared in other Ti/P ratios.

pH-controlled hydrothermal synthesis of titanium phosphates and their powder properties

Titanium phosphates were prepared from titanium chloride and sodium pyrophosphate at various pH in hydrothermal process as a novel white pigment for cosmetics.Their chemical composition,powder properties,photo catalytic activity,colour phase and smoothness were studied.The obtained materials had a higher Ti/P ratio than that used in preparation conditions because of the formation of titanium oxide and hydroxide.The samples prepared at pH=4 had particles smaller than 100μm.Titanium phosphates had less photo catalytic activity to protect the sebum on the skin.The obtained materials in hydrothermal process and their thermal products at 100℃showed high reflectance in the range of visible light.

Synthesis of nano SnO2-coupled mesoporous molecular sieve titanium phosphate as a recyclable photocatalyst for efficient decomposition of 2,4-dichlorophenol

It is essential to develop a cheap, recyclable, and efficient photocatalyst to help degrade pollutants contaminating the environment. Herein, mesoporous molecular sieve titanium phosphate （MMS-TiP） was used as an efficient nano-photocatalyst to degrade 2,4-dichlorophenol （2,4-DCP） and to oxidize CO. The catalyst was successfully synthesized by a simple and convenient hydrothermal method in the presence of a tri-block copolymer surfactant. Exceptional photoactivity of the optimized MMS-TiP mainly depends on its porous structure, with a large surface area by means of O2 temperature-programmed desorption curves and fluorescence spectra related to the amounts of produced hydroxyl radical. Interestingly, the photocatalytic activity of the prepared MMS-TiP could be greatly improved by coupling with nanocrystalline SnO2. This is likely due to the increase in the lifetime and separation of photogenerated charges by transferring electrons to SnO2 and was observed by steady-state surface photovoltage spectra and time-resolved surface photovoltage responses. The SnOa-coupled MMS-TiP exhibits better photocatalytic performance for 2,4-DCP degradation and better self-settlement than those of the commercial catalyst P25 TiO2. Moreover, it was confirmed by radical-trapping experiments that ·O2^- is the main activated species for the photocatalytic degradation of 2,4-DCP, and is photogenerated by electron transfer from MMS-TiP to SnO2. Furthermore, the main intermediates in the degradation of 2,4-DCP, like parachlorophenol superoxide and 1,2-benzenediol superoxide radicals, were detected, and a possible decomposition pathway related to ·O2^- attack is proposed. These experimental results provide new strategies for developing a recyclable molecular sieve- based nano-photocatalyst with high photocatalytic activity for environmental remediation.

Hydroxyapatite/β-tricalcium Phosphate Composite for Guiding Bone Tissue Growth into a Titanium Tube in 8 mm Dog Tibia Cavity Defects

We developed a fixation method and evaluate bone regrowth in the cavities of a Ф4 mm× 8 mm titanium（Ti）tube through porous hydroxyapatite（HAP）/β-tricalcium phosphate（β-TCP）composite filling（group A）,chitosan/calcium phosphate composite filling（group B）,and HAP particle modification（group C）.After 2 and 5 months of implantation in dog tibia defects,new bone formation in the three groups was studied by histology and histomorphometry.Group A displayed the most bone regenerated area in both 2 and 5 months post-operation.The chitosan/calcium phosphate composite in group B mostly degraded 2 months after implantation,leading to fibrous tissue invasion after 5 months.By contrast,less bone formation was observed in group C.These results indicated that filling the cavities of metalprostheses with a porous HAP/β-TCP composite can be used for stable long-term fixation in clinicalsettings.

A simple and novel synthetic route to prepare anatase TiO2 nanopowders from natural ilmenite via the H3PO4/NH3 process

A simple and novel technique for the preparation of anatase TiO2 nanopowders using natural ilmenite(FeTiO3)as the starting material is reported.Digesting ilmenite with concentrated H3PO4 under refluxing conditions yields a whiteα-titanium bismonohydrogen orthophosphate monohydrate(TOP),Ti(HPO4)2·H2O,which can be easily isolated via gravity separation from unreacted ilmenite.The addition of ammonia to the separated TOP followed by calcination at 500°C completes the preparation of anatase TiO2.Calcination at temperatures above 800°C converts the anatase form of TiO2 to the stable rutile phase.The removal of iron from ilmenite during the commercial production of synthetic TiO2 is problematic and environmentally unfriendly.In the present study,the removal of iron was found to be markedly simple due to the high solubility of iron phosphate species in concentrated H3PO4 with the precipitation of TOP.The titanium content of the prepared samples on metal basis with silica and phosphorous as major impurities was over 90%.Prepared TiO2 samples were characterized using X-ray fluorescence,Fourier-transform infrared spectroscopy,Raman spectroscopy,ultraviolet–visible diffuse reflectance spectroscopy,high-resolution transmission electron microscopy,and X-ray diffraction analyses.The photocatalytic potentials of the commercial and as-prepared TiO2 samples were assessed by the photodegradation of rhodamine B dye.

磷酸钛离子交换薄层色谱分离无机离子(英文)

The chromatographic behavior of 30 inorganic cations has been studied on thin layers of titanium phosphate ion-exchanger using several aqueous,organic and mixed mobile phases.The separation of one ion from several other ions and also ternary and binary separations have been developed.Some important analytical separations are reported.The effect of pH of the mobile phase on retention factor(Rf)values of the cations in the presence of complex-forming anion along with the separation power of the ion-exchanger were studied.This ion-exchanger exhibits high sorption capacity and varying selectivity towards metal ions and makes it a suitable stationary phase in thin layer chromatography.

Effect of Amino-,Methyl- and Epoxy-Silane Coupling as a Molecular Bridge for Formatting a Biomimetic Hydroxyapatite Coating on Titanium by Electrochemical Deposition

The objective of this study was to determine the role of functional groups of silane coupling on bioactive titanium （Ti） surface by electrochemical deposition, and calcium phosphate （CAP） coating, as well as bone cell adhesion and proliferation. Methyl group （-CH3）, amino group （-NH2）, and epoxy group （-glyph name--C（O）C） were introduced onto the bioactive Ti surface using self-assembled monolayers （SAMs） with different silane coupling agents as molecular bridges. The effect of the surface functional groups on the growth features of the CaP crystals was analyzed （including chemical compositions, element content, minerals morphology and crystal structure etc.）. CH3-terminated SAMs showed a hydrophobic surface and others were hydrophilic by contact angle measurement; NH2-terminated SAMs showed a positive charge and others were negatively charged using zeta-potential measurement. Scanning electron microscopy results confirmed that flower-like structure coatings consisting of various pinpoint-like crystals were formatted by different functional groups of silane coupling, and the CaP coatings were multicrystalline consisting of hydroxyapatite （HA） and precursors. CaP coating of CH3-terminated SAMs exhibited more excellent crystallization property as compared to coatings of --NH2 and -C（O）C groups. In vitro MC3T3- El cells adhesion and proliferation were performed. The results showed that CaP coatings on silane coupling functionalized surfaces supported cell adhesion and proliferation. Thus, these functional groups of silane coupling on Ti can form homogeneous and oriented nano-CaP coatings and provide a more biocompatible surface for bone regeneration and biomedical applications.

Combined quantitative microscopy on the microstructure and phase evolution in Li1.3Al0.3Ti1.7(PO4)3 ceramics

Lithium aluminum titanium phosphate(LATP)is one of the materials under consideration as an electrolyte in future all-solid-state lithium-ion batteries.In ceramic processing,the presence of secondary phases and porosity play an important role.In a presence of more than one secondary phase and pores,image analysis must tackle the difficulties about distinguishing between these microstructural features.In this study,we study the phase evolution of LATP ceramics sintered at temperatures between 950 and 1100℃by image segmentation based on energy-dispersive X-ray spectroscopy(EDS)elemental maps combined with quantitative analysis of LATP grains.We found aluminum phosphate(AlPO4)and another phosphate phase((Lix)PyOz).The amount of these phases changes with sintering temperature.First,since the grains act as an aluminum source for AlPO4 formation,the aluminum content in the LATP grains decreases.Second,the amount of secondary phase changes from more(Lix)PyOz at 950℃to mainly AlPO4 at 1100℃sintering temperature.We also used scanning electron microscopy(SEM)and confocal laser scanning microscopy(CLSM)to study the evolution of the LATP grains and AlPO4,and LATP grain size increases with sintering temperature.In addition,transmission electron microscopy(TEM)was used for the determination of grain boundary width and to identify the amorphous structure of AlPO4.