Electronic devices are produced from dielectric compositions comprising a mixture of precursor materials that, upon firing, forms a dielectric material comprising a barium-titanium-tungsten-silicon oxide.

An active material for a fluoride ion secondary battery includes a composite fluoride which contains: an alkali metal or NH.sub.4; a transition metal; and fluorine.

A method for producing a piezoelectric component is disclosed. In an embodiment, the method includes producing a ceramic precursor material of the general formula Pb.sub.1-x-y-(2a-b)/2V.sub.(2a-b)/2Ba.sub.xSr.sub.y[(Ti.sub.zZr.sub.1-z).sub.1-a-bW.sub.aRE.sub.b]O.sub.3, where RE is a rare earth metal and V is a Pb vacancy, mixing the ceramic precursor material with a sintering aid, forming a stack which includes alternating layers including the ceramic precursor material and a layer including Cu and debindering and sintering the stack thereby forming the piezoelectric component having Cu electrodes and at least one piezoelectric ceramic layer including Pb.sub.1-x-y-[(2a-b)/2]-p/2V.sub.[(2a-b)/2-p/2]Cu.sub.pBa.sub.xSr.sub.y[(Ti.sub.zZr.sub.1-z).sub.1-a-bW.sub.aRE.sub.b]O.sub.3, where 0x0.035, 0y0.025, 0.42z0.5, 0.0045a0.009, 0.009b0.011, and 2a>b, p2ab.

An apparatus and method for debindering a cellular ceramic green body. The apparatus includes a flow modulation member to selectively restrict circulation of a heated oxygen-containing atmosphere through a top of a cellular core section of the green body. The method includes heating the green body in a circulating oxygen-containing atmosphere while selectively restricting circulation of the atmosphere through the top of the cellular core section of the green body.

A method for firing a ceramic honeycomb body including heating a green ceramic honeycomb body from a first temperature to a second temperature at a first heating rate and at a first oxygen level. Then, the green ceramic honeycomb body is heated from the second temperature to a third temperature at a second heating rate and at a second oxygen level. In this firing schedule, the second heating rate is greater than the first heating rate, and the second oxygen level is greater than the first oxygen level. Further, oxygen is introduced into the kiln to increase an oxygen level of the kiln from the first oxygen level to the second oxygen level near a peak of organic volatile release.

The present disclosure provides methods to improve the properties of a porous structure formed by a rapid manufacturing technique. Embodiments of the present disclosure increase the bonding between the micro-particles 5 on the surface of the porous structure and the porous structure itself without substantially reduce the surface area of the micro-particles. In one aspect, embodiments of the present disclosure improves the bonding while preserving or increasing the friction of the structure against adjacent materials.

The present disclosure relates to the field of ceramics, and discloses a metal-based aluminum nitride composite material. The composite material includes an aluminum nitride ceramic skeleton and a metal filling at least part of pores of the aluminum nitride ceramic skeleton. The aluminum nitride ceramic skeleton contains aluminum nitride and CuAlO.sub.2, and the aluminum nitride ceramic skeleton has a porosity of 20 to 40 percent. The present disclosure further discloses a method for preparing the metal-based aluminum nitride composite material and the metal-based aluminum nitride composite material obtained by the method. A CuAlO.sub.2 substance is formed in the aluminum nitride ceramic skeleton obtained in the present disclosure.

The MnZn ferrite material includes principal components and auxiliary components, where the principal components include: 52.5 mol % to 53.8 mol % of Fe.sub.2O.sub.3, 8.8 mol % to 12 mol % of ZnO, and the balance of MnO; the auxiliary components include: 0.35 wt % to 0.5 wt % of Co.sub.2O.sub.3, 0.03 wt % to 0.08 wt % of CaSiO.sub.3, 0.01 wt % to 0.04 wt % of Nb.sub.2O.sub.5, and 0.05 wt % to 0.12 wt % of TiO.sub.2 and RE elemental components; the RE elemental components include one or more from the group consisting of 0 wt % to 0.04 wt % of Gd.sub.2O.sub.3, 0 wt % to 0.02 wt % of Ho.sub.2O.sub.3, and 0 wt % to 0.03 wt % of Ce.sub.2O.sub.3; the auxiliary components are all represented by a mass percentage relative to a total mass of the Fe.sub.2O.sub.3, the MnO, and the ZnO.

A preparation method of a high-thermal-conductivity and net-size silicon nitride ceramic substrate includes the following steps: (1) mixing an original powder, a sintering aid, a dispersant, a defoamer, a binder, and a plasticizer in a protective atmosphere to allow vacuum degassing to obtain a mixed slurry; (2) subjecting the mixed slurry to tape casting and drying in a nitrogen atmosphere to obtain a first green body; (3) subjecting the first green body to shaping pretreatment to obtain a second green body; (4) subjecting the second green body to debonding at 500? C. to 900? C. to obtain a third green body; and (5) subjecting the third green body to gas pressure sintering in a nitrogen atmosphere at 1,800? C. to 2,000? C. to obtain the high-thermal-conductivity and net-size silicon nitride ceramic substrate.

Provided herein are rapid, high quality film sintering processes that include high-throughput continuous sintering of lithium-lanthanum zirconium oxide (lithium-stuffed garnet). The instant disclosure sets forth equipment and processes for making high quality, rapidly-processed ceramic electrolyte films. These processes include high-throughput continuous sintering of lithium-lanthanum zirconium oxide for use as electrolyte films. In certain processes, the film is not in contact with any surface as it sinters (i.e., during the sintering phase).