Ceramic material and method of preparing the same

Abstract

A ceramic material, including: BaWO.sub.4-xM.sub.2CO.sub.3-yBaO-zB.sub.2O.sub.3-wSiO.sup.2, where x=0-0.2 mole, y=0-0.05 mole, z=0-0.2 mole, w=0-0.1 mole, M represents an alkali metal ion selected from Li.sup.+, K.sup.+, Na.sup.+, and x, y, z, and w are not zero at the same time.

Claims

1. A ceramic material, comprising: BaWO.sub.4-xM.sub.2CO.sub.3-yBaO-zB.sub.2O.sub.3-wSiO.sub.2, wherein x=0-0.2 mole, y=0-0.05 mole, z=0-0.2 mole, w=0-0.1 mole, M represents an alkali metal ion selected from Li.sup.+, K.sup.+, Na.sup.+, and x, y, z, and w are not zero at the same time.

2. A method, comprising: 1) weighing and mixing BaCO.sub.3, WO.sub.3, M.sub.2CO.sub.3, B.sub.2O.sub.3 and SiO.sub.2 based on a chemical formula BaWO.sub.4-xM.sub.2CO.sub.3-yBaO-zB.sub.2O.sub.3-wSiO.sub.2, wherein x=0-0.2 mole, y=0-0.05 mole, z=0-0.2 mole, w=0-0.1 mole, M represents an alkali metal ion selected from Li.sup.+, K.sup.+, Na.sup.+, and x, y, z, and w are not zero at the same time, to yield a first powder; 2) mixing the first powder obtained in 1), zirconia balls, and deionized water according to a mass ratio of 1:5:1-2, ball-milling for 4-7 h, drying at 80-120° C., sieving with a 40-60 mesh sieve, calcining in air atmosphere at 700-900° C. for 2-4 h, to yield a second powder; 3) mixing the second powder obtained in 2), zirconia balls, and deionized water according to a mass ratio of 1:5:1-2, ball-milling for 3-6 h, drying, to yield a third powder, and adding a binder to the third powder; and 4) compression molding a resulting product obtained in 3) under a pressure of 20 megapascal, drying at 400-500° C. and sintering at 850° C.-900° C. for 0.5-2 h.

3. The method of claim 2, wherein the binder is an acrylic solution.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The invention is described hereinbelow with reference to accompanying drawings, in which the sole FIGURE shows the X-ray diffraction patterns of ceramic materials in Examples 12 to 15.

DETAILED DESCRIPTION OF THE EMBODIMENTS

(2) To further illustrate, embodiments detailing a ceramic material are described below. It should be noted that the following embodiments are intended to describe and not to limit the disclosure.

(3) The chemical formula of the ceramic material is: BaWO.sub.4-xM.sub.2CO.sub.3-yBaO-zB.sub.2O.sub.3-wSiO.sub.2, x=0-0.2 mole, y=0-0.05 mole, z=0-0.2 mole, w=0-0.1 mole, where M represents alkali metal ion selected from Li.sup.+, K.sup.+, Na.sup.+, and x, y, z, and w cannot be equal to zero at the same time. The ceramic material is prepared via solid-state reaction method.

(4) The raw materials are: BaCO.sub.3, WO.sub.3, M.sub.2CO.sub.3, B.sub.2O.sub.3 and SiO.sub.2. This BaWO.sub.4 ceramic is prepared via a solid-state reaction, comprising:

(5) 1) weighing and mixing BaCO.sub.3, WO.sub.3, M.sub.2CO.sub.3, B.sub.2O.sub.3 and SiO.sub.2 based on a chemical formula BaWO.sub.4-xM.sub.2CO.sub.3-yBaO-zB.sub.2O.sub.3-wSiO.sub.2, wherein x=0-0.2 mole, y=0-0.05 mole, z=0-0.2 mole, w=0-0.1 mole, M represents an alkali metal ion selected from Li.sup.+, K.sup.+, Na.sup.+, and x, y, z, and w are not zero at the same time, to yield a first powder;

(6) 2) mixing the first powder obtained in 1), zirconia balls, and deionized water according to a mass ratio of 1:5:1-2, ball-milling for 4-7 h, drying at 80-120° C., sieving with a 40-60 mesh sieve, calcining in air atmosphere at 700-900° C. for 2-4 h, to yield a second powder;

(7) 3) mixing the second powder obtained in 2), zirconia balls, and deionized water according to a mass ratio of 1:5:1-2, ball-milling for 3-6 h, drying, to yield a third powder, and adding a binder to the third powder; and

(8) 4) compression molding a resulting product obtained in 3) under a pressure of 20 megapascal, drying at 400-500° C. and sintering at 850° C.-900° C. for 0.5-2 h.

(9) The microwave dielectric ceramics were prepared in the same procedures as described above. The relative dielectric constant and dielectric loss were measured with the Hakki-Coleman dielectric resonator method. The network analyzer (HP83752A, the United States) was switched to the TE011 mode. The τ.sub.f value was calculated according to the examined resonant frequency at 25° C. and 85° C.

(10) TABLE-US-00001 TABLE 1 Weights of raw materials in each example Examples 1 2 3 4 5 Mass of each BaCO.sub.3 22.774 23.279 23.073 23.176 22.572 raw material/g WO.sub.3 26.104 26.046 25.817 25.931 25.256 Li.sub.2CO.sub.3 — — — — — K.sub.2CO.sub.3 — — — — — Na.sub.2CO.sub.3 — — — — — B.sub.2O.sub.3 0.784 — 0.775 0.389 1.517 SiO.sub.2 0.338  0.675 0.335 0.504 0.655 Sintering temperature 850° C. Examples 6 7 8 9 10 Mass of each BaCO.sub.3 22.402 22.087 22.243 21.897 21.304 raw material/g WO.sub.3 25.676 25.316 25.495 25.099 24.418 Li.sub.2CO.sub.3 0.818 — — 1.600 — K.sub.2CO.sub.3 — 1.509 — — 2.911 Na.sub.2CO.sub.3 — — 1.166 — — B.sub.2O.sub.3 0.771 0.760 0.766 0.754 0.733 SiO.sub.2 0.333 0.328 0.330 0.650 0.633 Sintering temperature 875° C. Examples 11 12 13 14 15 Mass of each BaCO.sub.3 21.597 22.626 22.527 22.577 21.968 raw material/g WO.sub.3 24.754 26.582 26.465 26.524 25.809 Li.sub.2CO.sub.3 — 0.254 — — — K.sub.2CO.sub.3 — — 0.473 — — Na.sub.2CO.sub.3 2.263 — — 0.364 — B.sub.2O.sub.3 0.743 0.399 0.397 0.398 — SiO.sub.2 0.642 0.138 0.137 0.137 2.224 Sintering temperature 900° C.

(11) TABLE-US-00002 TABLE 2 Microwave dielectric properties of ceramic material in each example External diameter Thickness Tanδ Q × f τ.sub.f Examples (mm) (mm) εr (10.sup.−4) (GHz) (ppm/° C.) 1 11.01 6.99 8.69 4.58 20201 −24.10 2 10.75 6.37 8.24 4.98 19712 −26.56 3 10.71 6.65 8.11 4.67 20144 −21.14 4 10.80 6.25 8.13 4.70 20679 −22.36 5 10.66 5.66 7.06 5.14 21330 −20.02 6 10.79 5.95 6.88 5.28 21988 −20.56 7 10.82 5.83 6.69 6.12 18423 −22.37 8 10.69 6.07 7.32 6.33 17467 −23.22 9 10.83 6.17 6.25 4.37 24768 −15.13 10 10.76 5.87 6.00 4.80 22425 −12.71 11 10.61 6.25 6.60 4.33 23371 −19.36 12 10.99 5.63 8.15 5.58 23371 −25.10 13 11.02 5.55 8.30 3.98 32712 −26.56 14 10.70 6.06 7.98 7.23 17864 −21.14 15 10.50 5.65 7.50 3.70 37296 −22.36

(12) According to the tables, when the ceramics were sintered at 850° C.-900° C. for 0.5 h, all the samples possessed excellent properties, indicating that the materials can be applied to LTCC technology.

(13) The sole FIGURE represents the XRD patterns of ceramics (examples 12, 13, 14 and 15) sintered at 900° C. for 0.5 h. As shown, for y=0, only BaWO.sub.4 (JCPDS #01-072-0746) was observed, while in Example 15, BaWO.sub.4 (JCPDS #01-072-0746) and BaSi.sub.2O.sub.5 were detected.

(14) It will be obvious to those skilled in the art that changes and modifications may be made, and therefore, the aim in the appended claims is to cover all such changes and modifications.