Sintering synthesis method for nanometer negative expansion ceramic Zr2(WO4)(PO4)2

A synthesis method and negative expansion technology are applied in the field of sintering synthesis of nanometer negative expansion ceramic Zr22, which can solve the problems of long sintering time, long sintering time at high temperature and low product density, and achieve shortened sintering time, fast sintering speed and simple process. Effect

Inactive Publication Date: 2012-05-02
ZHENGZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Use ZrO 2 、WO 3 and NH 4 h 2 PO 4 or (NH 4 ) 2 HPO 4 Preparation of negative thermal expansion ceramic Zr 2 (WO 4 )(PO 4 ) 2 , but the NH released during pre-sintering at 900 °C 3 It will pollute the environment, and the sintering time at high temperature 1250°C is longer (8 h), and the final product density is lower
Due to the long sintering time at high temperature, the crystal growth particles are larger and the pores are more, resulting in a lower product density, which seriously affects the Zr 2 (WO 4 )(PO 4 ) 2 practical application of

Method used

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  • Sintering synthesis method for nanometer negative expansion ceramic Zr2(WO4)(PO4)2
  • Sintering synthesis method for nanometer negative expansion ceramic Zr2(WO4)(PO4)2
  • Sintering synthesis method for nanometer negative expansion ceramic Zr2(WO4)(PO4)2

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] The raw material ZrO 2 、WO 3 and P 2 o 5 Weigh it according to the stoichiometric ratio (molar ratio) Zr: W: P=2:1:2, grind it for about 0.5 h until uniform, and then add the raw material ZrO 2 、WO 3 and P 2 o 5 The total amount of 0.5 wt.% MgO, continue to grind for 1.5 h until uniform, and then at 150 o Dry at C for 6 h. After drying, grind for a few minutes to mix the raw materials evenly, and then press it into a cylinder with a diameter of 10 mm and a height of 10 mm with a uniaxial tablet press at a pressure of 300 MPa. Set up a high-temperature tube furnace to raise the temperature to a sintering temperature of 1350 °C, put the corundum crucible containing the sample into the tube furnace at the sintering temperature, sinter in normal pressure air for 10 min, take it out and quench in air. For the phase analysis of the X-ray diffraction (XRD) pattern corresponding to the product, see figure 1 , the XRD diffraction peak corresponds to PDF# 01-085-2239, indi...

Embodiment 2

[0027] The difference with embodiment 1 is: the sintering temperature is 1400 o C, the sintering time is 3 min. For the phase analysis of the XRD pattern corresponding to the product, see figure 2 , the XRD diffraction peak corresponds to PDF# 01-085-2239, indicating that the sample prepared in a short time is a pure phase of Zr 2 (WO 4 )(PO 4 ) 2 .

Embodiment 3

[0029] The difference from Example 2 is that the sintering time is 5 min, and the synthesized Zr 2 (WO 4 )(PO 4 ) 2 For the corresponding XRD phase analysis see image 3 , XRD results showed the formation of pure Zr 2 (WO 4 )(PO 4 ) 2 Mutually.

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Abstract

The invention discloses a sintering synthesis method for nanometer negative expansion ceramic Zr2(WO4)(PO4)2, which belongs to the field of inorganic non-metallic materials. According to the invention, ZrO2, WO3 and P2O5 are used as raw materials; the raw materials are weighed according to a stoichiometric ratio of Zr to W to P in the target product Zr2(WO4)(PO4)2 of 2: 1: 2; MgO which accounts for 0.5 to 1.5% of the total weight of the raw materials of ZrO2, WO3 and P2O5 is added, MgO and the raw materials are ground and uniformly mixed, then are dried, and then are ground and uniformly mixed again, and an obtained mixture is subjected to direct one-step sintering synthesis or to one-step sintering synthesis after performing, and a product obtained after sintering synthesis is quenched in the air so as to obtain the target product; wherein, sintering parameters are: temperature 1350 to 1450 DEG C, time 2 to 20 min. The invention has the advantages of a simple process, no pollution, a fast sintering speed and suitability for large scale production; Zr2(WO4)(PO4)2 has an average particle size in order of magnitude of hundreds of nanometers.

Description

technical field [0001] The invention belongs to the field of inorganic non-metallic materials, in particular to a nanometer negative expansion ceramic Zr 2 (WO 4 )(PO 4 ) 2 sintering synthesis method. Background technique [0002] In engineering materials, different materials must be used to meet the multifunctional requirements, but when the temperature changes, the thermal stress due to the difference in thermal expansion coefficient often causes performance degradation, temporary or permanent failure, shedding and fracture of materials or devices, etc. A series of problems, such as the drift of the central wavelength of the fiber Bragg grating with temperature, the systematic error of the thermal dilatometer, the degradation of the imaging quality caused by the change of the focal length of the space telescope with the temperature, the copper foil on the printed circuit board is detached due to heat, and the output beam of the laser due to the thermal lens effect Dive...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C04B35/495C04B35/622
Inventor 梁二军刘献省商瑞晁明举
Owner ZHENGZHOU UNIV
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