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Yong Yue

Bio: Yong Yue is an academic researcher. The author has contributed to research in topics: Hydrothermal synthesis & Hydrothermal circulation. The author has an hindex of 2, co-authored 3 publications receiving 17 citations.

Papers
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Journal ArticleDOI
TL;DR: A new potassium phosphatoantimonate was synthesized and characterized by means of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), differential thermal analysis (DTA), thermogravimetric analysis (TGA), infrared spectroscopy (IR), 31P solid-state NMR, and adsorption isothermal analysis as mentioned in this paper.
Abstract: A new potassium phosphatoantimonate was hydrothermally synthesized and characterized by means of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), differential thermal analysis (DTA), thermogravimetric analysis (TGA), infrared spectroscopy (IR), 31P solid-state NMR, and adsorption isothermal analysis. Results showed that this compound has a layered structure with the formula K8Sb8P2O29·8H2O. It crystallizes in the monoclinic system with unit-cell parameters a = 23.95(2) A, b = 9.51(5) A, c = 8.19(3) A, and β = 124.77°. The structure can be intercalated by organic amine molecules and the potassium ions located in between layers can be exchanged by monovalent ions. Factors such as the initial Sb/P molar ratio, pH, reaction temperature, and cations which dominate the hydrothermal synthesis of the product were assessed.

10 citations

Journal ArticleDOI
TL;DR: K3Sb3P2O14·5H2O was synthesized by a hydrothermal method, and characterized by X-ray diffraction (XRD), differential thermal analysis (DTA), thermogravimetry (TG) and 31P MAS NMR as mentioned in this paper.
Abstract: K3Sb3P2O14·5H2O was synthesized by a hydrothermal method, and characterized by X-ray diffraction (XRD), differential thermal analysis (DTA), thermogravimetry (TG) and 31P MAS NMR.

9 citations

Journal ArticleDOI
TL;DR: In this paper, the unit-cell parameters for K3Sb3P2O14·5H2O and K3sb3As2O 14·5h2O are compared to those for the corresponding phases synthesized by solid-state reactions.
Abstract: K3Sb3A2O14·5H2O (A P, As) were synthesized by use of a hydrothermal method, and the synthesis conditions are discussed in detail. Both phases were characterized by various techniques including scanning electron microscopy, XRD, XPS, 31P MAS NMR, IR, DTA–TG. The unit-cell parameters for K3Sb3P2O14·5H2O and K3Sb3As2O14·5H2O are slightly smaller than those for the corresponding phases synthesized by solid-state reactions.

Cited by
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Journal ArticleDOI
TL;DR: A personal account mainly based on recent results provides perspectives and new approaches that should be developed in the investigation of SCO materials.
Abstract: The spin-crossover phenomenon (SCO) is a fascinating field that potentially concerns any material containing a (d4–d7) transition metal complex finding therefore an echo in as diverse research fields as chemistry, physics, biology and geology. Particularly, molecular and coordination-polymers SCO solids are thoroughly investigated since their bistability promises new routes towards a large panel of potential applications including smart pigments, optical switches or memory devices. Notwithstanding these motivating applicative targets, numerous fundamental aspects of SCO are still debated. Among them, the investigation of the structure–property relationships is unfailingly at the heart of the SCO research field. All the facets of the richness of the structural behaviors shown by SCO compounds are only revealed when exploring the whole sample scales – from atomic to macroscopic – all the external stimuli – temperature, pressure, light and any combinations and derived perturbations – and the various forms of the SCO compounds in the solid state – crystalline powders, single-crystals, poorly crystalline or nano-sized particles. Crystallography allows investigating all these aspects of SCO solids. In the past few years, crystallography has certainly been in a significant phase of development pushing the frontiers of investigations, in particular thanks to the progress in X-ray diffraction techniques. The encounter between SCO materials and crystallography is captivating, taking advantages from each other. In this paper, a personal account mainly based on our recent results provides perspectives and new approaches that should be developed in the investigation of SCO materials.

171 citations

Book ChapterDOI
S.-H. Feng1, G.-H. Li1
01 Jan 2017
TL;DR: In this article, the authors introduce the foundation of hydrothermal and solvothermal syntheses, and describe the synthesis of some new materials including single crystals materials, zeolites and related microporous materials, ionic conductors, complex oxides and fluorides, inorganic-organic hybrid materials, and nanomaterials.
Abstract: Hydrothermal and solvothermal syntheses are important branches of inorganic synthesis. Hydrothermal and solvothermal techniques are not just confined to the syntheses and growth of conventional and advanced materials but also take a very broad shape, covering several interdisciplinary branches of science and widely applied in the fields of the treatment of wastes, mimicking geothermal and biohydrothermal processes. In this chapter, we introduce the foundation of hydrothermal and solvothermal syntheses, and we describe the hydrothermal synthesis of some new materials including single crystals materials, zeolites and related microporous materials, ionic conductors, complex oxides and fluorides, inorganic–organic hybrid materials, and nanomaterials. Hydrothermal biochemistry, supercritical water oxidation process, hydrothermal technique and methods, and ionothermal synthesis are also discussed.

106 citations

Book ChapterDOI
01 Jan 2011
TL;DR: In this article, the authors focus on the foundation of hydrothermal and solvothermal syntheses of materials, including the synthesis of conventional and advanced materials, treatment of wastes, and mimicking geothermal and bioehydrothermal processes.
Abstract: Publisher Summary This chapter focuses on the foundation of hydrothermal and solvothermal syntheses of materials, hydrothermal biochemistry, supercritical water oxidation process, technique and methods, and ionothermal synthesis. Hydrothermal and solvothermal syntheses are important branches of inorganic synthesis. Hydrothermal synthesis refers to the synthesis through chemical reactions in aqueous solution above boiling point of water and solvothermal synthesis in nonaqueous solution at relatively high temperatures. The development of hydrothermal and solvothermal techniques has a history, beginning with the synthesis of minerals and the extraction of elements from minerals. Nowadays, these techniques have widely been applied in the syntheses of conventional and advanced materials, treatment of wastes, and mimicking geothermal and bioehydrothermal processes. Zeolite and quartz industries further promote the basic studies of hydrothermal and solvothermal chemistry, and more and more scientists realize the importance of developing hydrothermal and solvothermal reactions, upon which effective syntheses would be established.

65 citations

Journal ArticleDOI
TL;DR: A new compound showing a large spin-crossover hysteresis spanning room temperature demonstrates in a definitive manner that this goal is achievable in molecular discrete compounds without damaging the single-crystal character.

42 citations

Journal ArticleDOI
Guangshe Li1, Shouhua Feng1, Lei Li1, Xirong Li1, Wei Jin1 
TL;DR: In this article, the structural stability and thermal properties of hydrogarnets were investigated by X-ray diffraction, DTA-TG, infrared, and Xray photoelectron spectroscopies.
Abstract: Hydrogarnets Sr3M2(OH)12 (M = Cr, Fe, and Al) were synthesized from mild hydrothermal systems at 240 °C with Sr(OH)2·8H2O, Cr(NO3)3·9H2O, Fe(NO3)3·9H2O, and Al(OH)3 as the starting materials. High solubility of the input species and basic concentration in the reaction systems considerably lower crystallization temperatures and enhance the crystallinity of the resulting hydrogarnets. The structural stability and thermal properties of Sr based hydrogarnets were investigated by X-ray diffraction, DTA-TG, infrared, and X-ray photoelectron spectroscopies. With increasing temperature, Sr based hydrogarnets underwent fast dehydration due to the loss of the nearest OH- species of Sr−OH dodecahedra. During the course of decomposition, valence variations of the hydrogarnet framework ions, e.g., Fe and Cr directly determined the decomposition process and phase compositions in final decomposition products. The decomposition product of Sr3Cr2(OH)12 in air was a mixture of SrCrO4 and SrO, but in N2, a mixture of a rhom...

32 citations