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Method for synthetizing synthetic metal boride nano-powder by iodine assisting magnesium co-reduction solid-phase reaction

A technology of metal borides and nanopowders, applied in the direction of metal borides, boron/borides, etc., can solve the problems of high temperature, high equipment requirements, high pressure, etc., and achieve the effect of low pressure, low price and low temperature

Inactive Publication Date: 2010-09-22
SHANDONG UNIV
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  • Summary
  • Abstract
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  • Claims
  • Application Information

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Problems solved by technology

For the preparation of ternary or multi-component borides, it is generally obtained by means of carbothermal, borothermal and thermite at high temperatures above 1000°C. Huo Dexuan and others can obtain multi-component metal hexaborides by using sodium borohydride and chloride, see CN200610053497.9 , as mentioned earlier, this method has high pressure and relatively high temperature. In practical application, the requirements for equipment are high, which is not conducive to large-scale production operations.
In addition, there are very few current reports on the preparation of multinary metal borides at milder temperatures.
And generally there are problems such as high cost of raw materials and difficulty in industrialization

Method used

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  • Method for synthetizing synthetic metal boride nano-powder by iodine assisting magnesium co-reduction solid-phase reaction
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  • Method for synthetizing synthetic metal boride nano-powder by iodine assisting magnesium co-reduction solid-phase reaction

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Embodiment Construction

[0011] Technical scheme of the present invention is as follows:

[0012] A method for synthesizing metal boride nanopowder by solid phase reaction, the metal boride includes rare earth metal hexaboride, alkaline earth metal hexaboride, transition metal boride or multiple boride, wherein,

[0013] The general formula of rare earth metal hexaboron compound and alkaline earth metal hexaboron compound is MB 6 , M=Sc, Y, Ce, Pr, Nd, Sm, Eu, Gd, Ca, Sr or, Ba;

[0014] The general formula of transition metal borides is M'B x , wherein x=1 or 2, M' is Ti, Zr, Hf, V, Nb or W;

[0015] Proceed as follows:

[0016] Put the metal source raw materials and boron source raw materials in an autoclave, and react at 170°C to 600°C for 30 minutes to 3 days under the co-reduction of reducing agent magnesium powder and auxiliary agent iodine; the initial product is treated with acid to remove impurities, filtered After drying, the pure-phase hexaboron compound nanopowder is obtained. Wherein...

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Abstract

The invention relates to a method for synthetizing synthetic metal boride nano-powder by iodine assisting magnesium co-reduction solid-phase reaction, which utilizes the iodine assisting magnesium co-reduction solid-phase reaction to synthetize alkaline earth, rare earth metal six-boron compound and transition metal boride as well as ternary rare earth six-boron compound, is a common and universal method, and can prepare and obtain YB6, ScB6, CeB6, PrB6, PrB6, NdB6, SmB6, EuB6, CaB6, SrB6, BaB6 and the like, ternary rare earth six-boron compound and transition metal boride.

Description

technical field [0001] The invention relates to a method for synthesizing metal borides by solid phase reaction, in particular to a method for synthesizing metal boride nanometer powder materials at relatively low temperature by using solid phase reaction of iodine-assisted magnesium co-reduction in a reactor. Background technique [0002] Boron compounds of transition metals and hexaboron compounds of alkaline earth and rare earth metals have high hardness, high melting and boiling points, and good thermal and chemical stability. Rare earth and alkaline earth metal hexaboron compounds have low work functions and are generally good field emission materials. Niobium boride and yttrium hexaboride are superconductors. Due to the above-mentioned excellent properties of boron compounds, the synthesis of borides has aroused the interest of scientists. So far, a variety of synthetic routes have been developed, such as direct synthesis of elements at 1800°C (J.Cryst.Growth 11(1971...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B35/04
Inventor 钱逸泰王连成马小健
Owner SHANDONG UNIV
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