发明名称 |
Process for preparing various morphology NTE compound ZrW<sub>0.5</sub>Mo<sub>1.5</sub>O<sub>8</sub> |
摘要 |
A process for preparing various morphology NTE compound ZrW0.5Mo1.5O8 comprising: preparing 0.4M Zr4+ solution, 0.2M W6+ solution and 0.6M Mo6+ solution with zirconyl nitrate, ammonium tungstate and ammo-nium molybdate separately, mixing them with the same volume and stirring until they are mixed well, adding 6-12M hydrochloric acid with the volume of 1/5-1/7 of the mixed solution, or adding 6-12M hydrochloric acid with the volume of 1/3-1/5 of the mixed solution and 0.2-0.4 wt % ammonium monoacid phosphate of all raw materials, or adding 9-18M sulfuric acid with the volume of 1/10-1/5 of the mixed solution, well mixing, transferring the mixed solution into the hydrothermal reactor, reacting at 150-180° C. for 8-25 hours, washing, drying and getting the precursor, heating the precursor at 480-500° C. for more than 5 hours and obtaining the product is provided. |
申请公布号 |
US9090480(B2) |
申请公布日期 |
2015.07.28 |
申请号 |
US200913320137 |
申请日期 |
2009.08.27 |
申请人 |
JIANGSU UNIVERSITY |
发明人 |
Cheng Xiaonong;Yang Juan;Liu Qinqin;Sun Xiujuan;Xu Guifang |
分类号 |
C30B29/22;C01G41/00;B82Y30/00 |
主分类号 |
C30B29/22 |
代理机构 |
Schmeiser, Olsen & Watts, LLP |
代理人 |
Schmeiser, Olsen & Watts, LLP |
主权项 |
1. A method for preparing various morphology NTE compound ZrW0.5Mo1.5O8 comprising the steps of:
preparing a 0.4M Zr4+ solution, a 0.2M W6+ solution and a 0.6M Mo6+ solution with zirconyl nitrate, ammonium tungstate and ammonium molybdate separately, mixing the 0.4M Zr4+ solution, a 0.2M W6+ solution and a 0.6M Mo6+ solution with a same volume and stirring until at least one of the 0.4M Zr4+ solution, the 0.2M W6+ solution, and the 0.6M Mo6+ solution are mixed well to obtain a first mixed solution; after stirring, adding 6M hydrochloric acid with a volume of 1/3 of the first mixed solution and adding a 0.2 wt % ammonium monoacid phosphate of all raw materials into the first mixed solution and well mixing to obtain a second mixed solution; transferring the second mixed solution into a hydrothermal reactor and placing into an oven and reacting the second mixed solution for 18 hours at 180° C., followed by repeated washings with deionized water and drying at 50˜80° C. to obtain a precursor ZrW0.5Mo1.5O7(OH)2(H2O)2; and heating the precursors at 490° C. for 6 hours to obtain a final product nanobundle-lile ZrW0.5Mo1.5O8. |
地址 |
CN |