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30results about How to "Lower the burn-in temperature" patented technology

High-performance permanent ferrite and dyadic manufacturing method thereof

The invention discloses a high-performance permanent magnetic ferrite and a binary production method thereof. The permanent magnetic ferrite is prepared from a material A, a material B and a ball milling additive with accessories. The contents of the ingredients by weight are as follows: 67-90 percent of material A, 9-30 percent of material B and 1-3 percent of ball milling additive; the material A is the once preburning material of strontium ferrite purchased from the market; the material B comprises the following ingredients by weight (the total being 100 percent): 79.0-83.0 percent of ferric oxide with the purity of Fe2O3 of not less than 98.5 percent and the purity of SiO2 of not more than 0.05 percent, 5.0-9.0 percent of lanthana with the purity of La2O3 of not less than 98 percent, 9.0-13.0 percent of strontium carbonate with the purity of SrCO3 of not less than 97.5 percent and 2.7-3.3 percent of cobaltosic oxide with the purity of Co3O4 of not less than 98 percent. The material B is obtained through batching, mixing, drying, dispersing, preburning, grinding and sieving. The invention has the advantages of high magnetic performance of products, relatively low cost, strong market competitiveness, easy forming of magnetic pieces and the like and can be widely applied to the production process of high-performance permanent magnetic ferrite.
Owner:SINOSTEEL ANHUI TIANYUAN TECH

Lead manganate niobate-lead nickelate niobate-lead zirconate titanate high-voltage ferroelectric ceramic with ultralow dielectric loss and preparation method thereof

The invention relates to lead manganate niobate-lead nickelate niobate-lead zirconate titanate high-voltage ferroelectric ceramic with ultralow dielectric loss and a preparation method thereof. The invention belongs to the field of ferroelectric materials. The invention aims to solve the technical problem of high dielectric loss of an existing soft ceramic. The chemical general formula of the lead manganate niobate-lead nickel niobate-lead zirconate titanate high-voltage electric ferroelectric ceramic with ultralow dielectric loss is x Pb (Mn1/3Nb2/3) O3-(0.55-x) Pb (Ni1/3Nb 2/3) O3-0.135 PbZrO3-0.315 PbTiO3, wherein x is equal to 0.01-0.03. The preparation method comprises the following steps of: proportioning components according to the proportion of the ceramic components; sequentially carrying out pre-sintering, tabletting, glue discharging and sintering; carrying out silver sintering and polarization to obtain the lead manganate niobate-lead nickelate niobate-lead zirconate titanate high-voltage ferroelectric ceramic with ultralow dielectric loss. According to the method, the pre-sintering temperature is low, the lead manganate niobate-lead nickelate niobate-lead zirconate titanate relaxor ferroelectric ceramic is sintered through optimization of a formula and a process, the piezoelectric constant of the ceramic, measured by a quasi-static d33 tester reaches 760 pC/N, meanwhile, the dielectric loss of the ceramic is lower than 0.5%, and the performance of the ceramic is excellent.
Owner:HARBIN INST OF TECH

Anion substituted low-temperature sintered lithium magnesium and titanium series microwave dielectric ceramic

The invention belongs to the technical field of ceramic materials, and discloses an anion substituted low-temperature sintered lithium magnesium and titanium series microwave dielectric ceramic and apreparation method thereof. The chemical formula of the anion substituted low-temperature sintered lithium magnesium and titanium series microwave dielectric ceramic is Li2Mg3Ti (O1-x/2Fx)6, and 0.06</=x</=0.12. The preparation method comprises the steps of blending Li2CO3, MgO, TiO2 and LiF in proportion; drying and sieving after primary ball-milling, and calcining at a certain temperature to obtain pre-calcined powder; after secondarily ball-milling the pre-calcined powder, drying and sieving the pre-calcined powder, granulating the pre-calcined powder, sieving, and then compressing to obtain a blank; and sintering the blank at a certain temperature, and after insulating, cooling the product to the room temperature to obtain the final product. A traditional solid-phase method is adopted,by substitution of F-ions to O2-ions, the pre-calcining temperature and sintering temperature of the lithium magnesium and titanium ceramic are reduced effectively, the low-temperature sintered Li2Mg3TiO6 series microwave dielectric ceramic is prepared, meanwhile, an excellent microwave dielectric property is maintained, and application of the ceramic in an LTCC technology can be met.
Owner:TIANJIN UNIV

Coprecipitation preparation method for calcium barium zirconate titanate leadless piezoelectric ceramic material

The invention discloses a coprecipitation preparation method for a calcium barium zirconate titanate leadless piezoelectric ceramic material. The method comprises the following steps: using barium acetate, calcium acetate, zirconium nitrate and titanium tetrachloride as raw materials, using sodium hydroxide or potassium hydroxide as a precipitator, firstly preparing calcium barium zirconate titanate precursor powder with high purity, uniform particles and relatively high activity, and then carrying out presintering, pelleting, tabletting, glue arrangement and sintering on the precursor to obtain the calcium barium zirconate titanate leadless piezoelectric ceramic material. Presintered powder of the ceramic material is prepared by adopting a coprecipitation method, the technology is simple and low in cost, no impurity is unlikely to introduce in the whole process, the prepared presintered powder is high in purity, uniform in dispersion, uniform in shape and relatively high in activity, the sintering temperature is reduced, and meanwhile the sintering temperature of the ceramic material can also be reduced, so that the problem that a traditional solid-phase method is non-uniform in mechanical mixing, unlikely to introduce impurities and high in synthesis temperature is solved.
Owner:SHAANXI NORMAL UNIV

Nine-layer-structure titanium iron bismuth cobalt oxide multiferroic ceramic material and preparation method thereof

The invention discloses a nine-layer-structure titanium iron bismuth cobalt oxide ceramic material with multiferroic performance and a preparation method thereof. The preparation method is characterized in that dissolving titanate, bismuth nitrate, ferric nitrate and cobalt nitrate in an aqueous nitric acid solution according to a mol ratio of 3: 10: (6-x): x and adding a complexing agent composed of ethylene diamine tetraacetic acid and citric acid, wherein a mol ratio of ethylene diamine tetraacetic acid to citric acid to metal ions in the solution is 0.5-1: 1: 1; and pre-burning powder obtained after full evaporation of the solution at a temperature of 700 to 800 DEG C to remove an organic matter and carrying out sintering at a temperature of 800 to 1100 DEG C for 5 to 10 h after tablet compressing and molding so as to obtain a nine-layer-structure Aurivillius-type multiferroic ceramic with a chemical formula of Bi10Fe6-xCoxTi3O30. The structure of the ceramic is that three titanium-oxygen (Ti-O) octahedrons and six iron-oxygen (Fe-O) octahedrons are sandwiched between two bismuth-oxygen layers ((Bi2O2)<2+>) and a part of Fe is substituted by Co; and the ceramic has ferroelectricity and ferromagnetism at the same time at a temperature higher than room temperature.
Owner:UNIV OF SCI & TECH OF CHINA

A kind of double niobium source alkali metal niobate micro-nanowire material and preparation method thereof

The invention discloses a double niobium source alkali metal niobate micro-nano wire material, with K 2 CO 3 、Na 2 CO 3 , Nb 2 o 5 、C 10 h 5 NbO 20 、BaCO 3 、 Bi 2 o 3 as raw material, according to the chemical formula (1‑ y )K z Na 1‑ z Nb (C)x Nb (N)1‑x o 3 - y BaBiO 3 For batching, where Nb (C) Refers to the niobium source C 10 h 5 NbO 20 Nb element; Nb (N) Refers to the niobium source Nb 2 o 5 Nb element; 0< x ≤0.1, 0< y <0.1,0.4≤ z ≤0.6, micro-nano wire material synthesized by traditional ceramic solid-phase sintering process. The preparation method comprises the following steps: 1) drying raw materials; 2) weighing raw materials and performing ball milling; 3) pre-calcining the powder after ball milling; 4) second ball milling of the powder after pre-calcining; 5) pressing into a circle billet; 6) insulation treatment of round billet. The advantage of the present invention is that the crystallinity of the green compact powder and the growth rate of the micro-nano wires can be increased after the double niobium source is used; at the same time, pure water can be used as the ball milling medium without the use of absolute ethanol, which greatly saves costs and reduces Pollution to the environment and potential safety hazards in the drying process.
Owner:GUILIN UNIV OF ELECTRONIC TECH

An ultra-low dielectric loss lead niobate manganate-lead niobate nickelate-lead zirconate titanate high piezoelectric ferroelectric ceramic and its preparation method

An ultra-low dielectric loss lead niobate-lead niobate-nickelate-lead zirconate titanate high-voltage ferroelectric ceramic and a preparation method thereof. The invention belongs to the field of piezoelectric ferroelectric materials. The invention aims to solve the technical problem of high dielectric loss of existing soft ceramics. The general chemical formula of a kind of lead niobate manganate-lead niobate-nickelate-lead zirconate titanate high piezoelectric ferroelectric ceramic of the present invention is x Pb(Mn 1 / 3 Nb 2 / 3 )O 3 ‑(0.55‑x)Pb(Ni 1 / 3 Nb 2 / 3 )O 3 ‑0.135PbZrO 3 ‑0.315PbTiO 3 , where x=0.01‑0.03. Preparation method: according to the proportion of ceramic ingredients, then pre-fired, pressed, deglued, sintered, and then silver-fired and polarized to obtain lead niobate-manganate-lead niobate-zirconate with ultra-low dielectric loss Lead titanate piezoelectric ferroelectric ceramics. The method of the present invention has a low pre-firing temperature, and the lead niobate-manganese-niobate-lead-niobinickelate-lead zirconate-titanate relaxor ferroelectric ceramics are obtained by optimizing the formula and process, and the quasi-static d 33 While the piezoelectric constant measured by the tester reaches 760pC / N, the dielectric loss is lower than 0.5%, and the performance is excellent.
Owner:江苏省声学产业技术创新中心

Dual-niobium-source alkali metal niobate micro-nano wire material and preparation method thereof

The invention discloses a dual-niobium-source alkali metal niobate micro-nano wire material. The micro-nano wire material is synthesized through a traditional ceramic solid-phase sintering process byusing K2CO3, Na2CO3, Nb2O5, C10H5NbO20, BaCO3 and Bi2O3 as raw materials which are blended according to a chemical formula of (1-y)K<z>Na<1-z>Nb<(C)x>Nb<(N)1-x>O<3-y>BaBiO<3>, wherein Nb<(C)> is an element Nb from a niobium source C<10>H<5>NbO<20>, Nb<(N)> is an element Nb from a niobium source Nb<2>O<5>, x is greater than 0 and less than or equal to 0.1, y is greater than 0 and less than 0.1, andz is greater than or equal to 0.4 and less than or equal to 0.6. A preparation method of the dual-niobium-source alkali metal niobate micro-nano wire material comprises the following steps of (1) rawmaterial drying; (2) raw material weighing and ball-milling; (3) pre-sintering of powder obtained after ball-milling; (4) secondary ball-milling of pre-sintered powder; (5) pressing of powder obtained after secondary ball-milling into a round billet; (6) heat preservation treatment of the round billet. The dual-niobium-source alkali metal niobate micro-nano wire material and the preparation method thereof have the advantages that after the double niobium sources are adopted, the crystallinity of pressed billet powder and the growth speed of micro-nano wires can be effectively increased; meanwhile, purified water can be used as a ball-milling medium, no absolute ethyl alcohol is needed, and thus the cost is greatly saved and environment pollution and potential safety hazards in the dryingprocess are reduced; the pre-sintering temperature is lowered by 150-425 DEG C, and heat preservation time is shortened.
Owner:GUILIN UNIV OF ELECTRONIC TECH
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