Patent classifications
C04B2235/3852
Ceramic nuclear fuel having UB2 enriched in 11B
A fuel assembly for a nuclear reactor, a fuel rod of the fuel assembly, and a ceramic nuclear fuel pellet of the fuel rod are disclosed. The fuel pellet includes a first fissile material of UB.sub.2, The boron of the UB.sub.2 is enriched to have a concentration of the isotope .sup.11B that is higher than for natural B.
Tuning the piezoelectric and mechanical properties of the ALN system via alloying with YN and BN
Methods and materials are disclosed for simultaneously optimizing both the piezoelectric and mechanical properties of wurtzite piezoelectric materials based on the AlN wurtzite and alloyed with one or two end-members from the set BN, YN, CrN, and ScN.
Method for producing ceramic sintered body, ceramic sintered body, and light emitting device
Provided are a method for producing a ceramic sintered body having improved light emission intensity, a ceramic sintered body, and a light emitting device. The method for producing a ceramic sintered body comprises preparing a molded body that contains a nitride fluorescent material having a composition containing: at least one alkaline earth metal element M.sup.1 selected from the group consisting of Ba, Sr, Ca, and Mg; at least one metal element M.sup.2 selected from the group consisting of Eu, Ce, Tb, and Mn; Si; and N, wherein a total molar ratio of the alkaline earth metal element M.sup.1 and the metal element M.sup.2 in 1 mol of the composition is 2, a molar ratio of the metal element M.sup.2 is a product of 2 and a parameter y and wherein y is in a range of 0.001 or more and less than 0.5, a molar ratio of Si is 5, and a molar ratio of N is 8, and wherein the nitride fluorescent material has a crystallite size, as calculated by X-ray diffraction measurement using the Halder-Wagner method, of 550 Å or less, and calcining the molded body at a temperature in a range of 1,600° C. or more and 2,200° C. or less to obtain a sintered body.
SPUTTERING TARGET AND METHOD FOR MANUFACTURING THE SAME
A novel metal oxide or a novel sputtering target is provided. A sputtering target includes a conductive material and an insulating material. The insulating material includes an oxide, a nitride, or an oxynitride including an element M1. The element M1 is one or more kinds of elements selected from Al, Ga, Si, Mg, Zr, Be, and B. The conductive material includes an oxide, a nitride, or an oxynitride including indium and zinc. A metal oxide film is deposited using the sputtering target in which the conductive material and the insulating material are separated from each other.
DENTAL ZIRCONIA TREATMENT TECHNOLOGY
The present disclosure relates to the field of dental material treatment, and particularly to a dental zirconia treatment technology. The specific technical solution is as follows: a zirconia treatment method, mainly involving color masking the zirconia, surface roughening the zirconia, coloring the zirconia, surface protection treatment and additional protective film treatment. Based on this treatment method, a brand-new color masking liquid, coloring liquid and adhesive solution are proposed. The present zirconia treatment technology not only meets the individualized requirements of patients for teeth, but also meets the requirements of dentists for convenient operation, so that it is of great value in application and popularization on the market.
CUBIC BORON NITRIDE SINTERED MATERIAL
A cubic boron nitride sintered material includes: more than 80 volume % and less than 100 volume % of cubic boron nitride grains; and more than 0 volume % and less than 20 volume % of a binder phase. The binder phase includes: at least one selected from a group consisting of a simple substance, an alloy, and an intermetallic compound selected from a group consisting of a group 4 element, a group 5 element, a group 6 element in a periodic table, aluminum, silicon, cobalt, and nickel. A dislocation density of the cubic boron nitride grains is more than or equal to 3×10.sup.17/m.sup.2 and less than or equal to 1×10.sup.20/m.sup.2.
Method for manufacturing a hole jewel
A method for manufacturing a hole jewel, including forming a precursor from a mixture of at least one powder material with a binder; pressing the precursor, with upper lower dies, to form a green body of the future hole jewel including a blind cavity having a height between a height of the green body and a height of the future hole jewel, the cavity being provided with upper and lower portions respectively including blanks of a through hole and of a functional element of the future hole jewel; sintering the green body to form a body of the future hole jewel; machining the body, including a first sub-step of shaping a top of the body, during which a height of the upper portion is configured in readiness for an opening in the through hole blank for connecting the functional element to the upper surface, and a second sub-step of shaping a base of the body to form a lower surface of the hole jewel for connecting the functional element to to the lower surface.
ELASTOMER-DERIVED CERAMIC STRUCTURES AND USES THEREOF
The disclosure relates to, among other things, an abrasive article comprising a plurality of 4D-ceramic structures, wherein the 4D-ceramic structures are made by a method comprising sequentially: at least partially removing a strain from a second strained primary polymer ceramic precursor, comprising a polymeric substrate and ceramic precursor particles dispersed therein, to give a 4-D ceramic precursor comprising a polymeric substrate; and thermolytically removing the polymeric substrate from the 4-D ceramic precursor comprising a polymeric substrate to provide a 4D-ceramic structure.
Cubic boron nitride sintered material
A cubic boron nitride sintered material comprises 30% by volume or more and 80% by volume or less of cubic boron nitride grains and 20% by volume or more and 70% by volume or less of a binder phase, the cubic boron nitride grains having a dislocation density of 3×10.sup.17/m.sup.2 or more and 1×10.sup.20/m.sup.2 or less.
MATERIALS FOR AMMONIA SYNTHESIS
Disclosed herein are doped perovskite oxides. The doped perovskite oxides may be used as a cathode material in an electrochemical cell to electrochemically generate ammonia from N.sub.2. The doped perovskite oxides may be combined with nitride compounds, for instance iron nitride, to further increase the efficiency of the ammonia production.