Synthesis of yttria nano-powders by the precipitation method: The influence of ammonium hydrogen carbonate to metal ions molar ratio and ammonium sulfate addition

2016 ◽  
Vol 678 ◽  
pp. 258-266 ◽  
Author(s):  
Shanshan Li ◽  
Binglong Liu ◽  
Jiang Li ◽  
Xingwen Zhu ◽  
Wenbin Liu ◽  
...  
2014 ◽  
Vol 1015 ◽  
pp. 350-354
Author(s):  
Li Na Chen ◽  
Wan Yi Liu ◽  
Qi Lin Hu

Contraposing the waste anolyte of industry, the paper proposed a new chemical precipitation method to recover Mn (II) ions and Mg (II) ions from the waste solution using ammonium hydrogen carbonate and ammonium dihydrogen phosphate as precipitants, respectively. The technological conditions of dealing procedure such as the molar ratio of reactants, pH value, reaction temperature and time, aging time were investigated. The results shown that the removal rate of Mn (II) ions and Mg (II) ions reached to 96 % and 98 %, and the yields of MnCO3 and NH4MgPO4·6H2O reached to 91 % and 94 %, respectively. The residual solution was recycled to realize the treatment greenly, which could meet the needs of production and increase environmental benefits.


2012 ◽  
Vol 512-515 ◽  
pp. 24-27 ◽  
Author(s):  
Hui Feng Lu ◽  
Ming Li Qin ◽  
Sui He Jiang ◽  
Ai Min Chu ◽  
Yan Zhang ◽  
...  

Abstract. Aluminum nitride(AlN) powders were synthesized by carbonthermal reduction of Ammonium aluminum carbonate hydroxide(AACH). The AACH were prepared from ammonium alum and ammonium hydrogen carbonate by precipitation method and AACH adhere to carbon black during precipitation. The precursor has a high reaction activity (near 100% of nitridation ratio after heated in flow nitrogen at 1400°C, 2h). After carbon remove in muffle furnace at 700 °C, white color Aluminum nitride (AlN) powder attained and mean size is 100 nm. The specific surface area of the powders decreased with increasing of concentration of ammonium alum and ammonium hydrogen carbonate, which range from 22 m2/g to 7 m2/g, particle size vary from 58 to 120 nm. Phase presents in the products during heating in flowed nitrogen were observed by X-ray diffraction. The -Al2O3 formed when the precursor heated to 1200°C, AlN was founded at 1300°C and the reaction ended at 1400°C, the reaction temperature and annealing time were much lower than nitridate the mixture of Al2O3 and carbon black. Particle size was increased when reaction temperature increased from 1400°C to 1550°C.


2016 ◽  
Vol 690 ◽  
pp. 224-229 ◽  
Author(s):  
Adison Saelee ◽  
Sirithan Jiemsirilers ◽  
Supatra Jinawath ◽  
Karn Serivalsatit

Magnesium aluminate spinel (MgAl2O4) is widely used in many engineering applications due to its high melting point (2135°C), high mechanical strength, chemical inertness, and good optical properties. Precipitation method is recognized as a convenient and cost-effective method for the synthesis of nanopowders. In this present work, MgAl2O4 nanopowders were prepared by precipitation method using ammonium hydrogen carbonate as a precipitant. The precipitated precursors were a mixture of ammonium dawsonite (NH4Al (OH)2CO3·H2O) and hydrotalcite (Mg6Al2(CO3)(OH)16·4H2O). After calcining at 1100°C for 2 hours, The MgAl2O4 nanopowders with particle size of 20-170 nm were obtained. The sinterability of the MgAl2O4 nanopowders was evaluated by sintering compacts of the MgAl2O4 nanopowders at temperature of 1300-1650°C for 2 hours. The relative density of the sintered MgAl2O4 ceramics reached about >97% of theoretical density after sintering at 1500°C for 2 hours. The Vicker’s hardness of the sintered ceramics reached a value of 1414 HV (13.9 GPa) after sintering at 1650°C for 2 hours.


2020 ◽  
Vol 7 (1) ◽  
pp. 6
Author(s):  
Dianjun Hu ◽  
Xin Liu ◽  
Ziyu Liu ◽  
Xiaoying Li ◽  
Feng Tian ◽  
...  

As a kind of promising material for a Faraday isolator used in the visible and near infrared range, Dy2O3 transparent ceramics were prepared by vacuum sintering from the nano-powders synthesized by the liquid precipitation method using ammonium hydrogen carbonate as precipitant with no sintering aids. The synthesized precursor was calcinated at 950 °C–1150 °C for 4 h in air. The influences of the calcination temperature on the morphologies and phase composition of Dy2O3 powders were characterized. It is found that the Dy2O3 powder calcinated at 1000 °C for 4 h is superior for the fabrication of Dy2O3 ceramics. The Dy2O3 transparent ceramic sample prepared by vacuum sintering at 1850 °C for 10 h, and subsequently with air annealing at 1400 °C for 10 h, from the 1000 °C-calcined Dy2O3 powders, presents the best optical quality. The values of in-line transmittance of the optimal ceramic specimen with the thickness of 1.0 mm are 75.3% at 2000 nm and 67.9% at 633 nm. The Verdet constant of Dy2O3 ceramics was measured to be −325.3 ± 1.9 rad/(T·m) at 633 nm, about 2.4 times larger than that of TGG (Tb3Ga5O12) single crystals.


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