623 results about "Strontium oxide" patented technology

A catalyst system and a method for reducing nitrogen oxides in an exhaust gas by reduction with a hydrocarbon or oxygen-containing organic compound reducing agent are provided. The catalyst system contains a silver catalyst and a modifier catalyst, where the modifier catalyst contains a modifier oxide, where the modifier oxide is selected from the group consisting of iron oxide, cerium oxide, copper oxide, manganese oxide, chromium oxide, a lanthanide oxide, an actinide oxide, molybdenum oxide, tin oxide, indium oxide, rhenium oxide, tantalum oxide, osmium oxide, barium oxide, calcium oxide, strontium oxide, potassium oxide, vanadium oxide, nickel oxide, tungsten oxide, and mixtures thereof. The modifier oxide is supported on an inorganic oxide support or supports, where at least one of the inorganic oxide supports is an acidic support. The catalyst system of the silver catalyst and the modifier catalyst provides higher NOx conversion than either the silver catalyst or the modifier catalyst alone.

An organic electroluminescent device having high efficiency, a long life time, and low cost, includes a substrate, a hole injecting electrode and an electron injecting electrode formed on the substrate, an organic material-containing organic layer between the electrodes, and an inorganic insulative electron injecting and transporting layer between the light emitting layer and the electron injecting electrode. The organic layer includes a light emitting layer containing a conjugated polymer, and the inorganic insulative electron injecting and transporting layer comprises three components. The first component is at least one oxide selected from the group consisting of lithium oxide, rubidium oxide, potassium oxide, sodium oxide, and cesium oxide. The second component is at least one of strontium oxide, magnesium oxide, and calcium oxide. The third component consists of silicon oxide, germanium oxide, or mixtures thereof.

The present invention relates to an optical glass using silicic acid group as main body, said optic glass has high expansion coefficient, high Young modulus, excellent weatherability and high transmissivity in the infrared wave zone. Said glass composition contains (mole%) 36-66% of silicon dioxide, 0-12% of aluminium oxide, 0-6% of boric oxide, 0-10% of magnesium oxide, 0-16% of calcium oxide, 0-16% of strontium oxide, 0-16% of baria, 0-8% of zinc oxide, 0-32% of lithium oxide, 0-25% of sodium oxide, 0-25% of potassium oxide, 0-20% of cesium oxide, 0-6% of phosphorus pentoxide, 0-8% of scandium oxide and others.

A sintering aid for a low-temperature cofired medium ceramic material is composed of, by weight, 31%-45% of silicon dioxide, 1%-10% of boron oxide, 5.1%-10% of zinc oxide, 18%-30% of aluminum oxide, 11%-24% of alkaline earth metallic oxide and 5%-15% of oxide with the general formula of R2O3, wherein R refers to at least one of lanthanum, cerium, praseodymium, neodymium, samarium, europium and dysprosium, and the alkaline earth metallic oxide refers to one of magnesium oxide, calcium oxide, barium oxide and strontium oxide. Adding the sintering aid into the low-temperature cofired medium ceramic material enables the prepared low-temperature cofired medium ceramic to have excellent thermal mechanical performance and dielectric performance. In addition, the invention provides the low-temperature cofired medium ceramic material and application thereof and a method for preparing the low-temperature cofired medium ceramic.

The invention relates to a permanent ferrite magnetic arc and the manufacturing method thereof, belonging to a manufacturing field of a motor permanent ferrite. Weight proportions of main material components and additive components are as the following: main materials: 8.7 to 9.0 percent of strontium oxide; 86 to 87 percent of iron oxide red; additives: 0.6 to 1.0 percent of calcium carbonate; 0.6 to 1.0 percent of aluminum oxide; 0.4 to 0.8 percent of chrome oxide; 0.3 to 0.6 percent of boric acid; 0.3 to 0.5 percent of silicon oxide; 0.2 to 0.4 percent of cobalt oxide; 0.2 to 0.4 percent of lanthanum oxide and 0.1 to 0.3 percent of silicate fiber. The invention is provided with high surplus magnetic induction strength and high intrinsic coercivity so as to enhance a mechanical strength of the magnetic arc.

A process for the preparation of an organosilicon condensate which comprises reacting together a silicon containing compound having at least one silanol group and a silicon containing compound having at least one —OR group or at least one silanol group (or a compound having both groups) in the presence of strontium oxide, barium oxide, strontium hydroxide or barium hydroxide and optionally a solvent such as water, methanol, ethanol, 1-propanol, 2-propanol, 1-butanol and 2-butanol, acetone or toluene.

An object of the invention is to achieve an organic EL device which is resistant to a deterioration of an inorganic-organic interface, has performance equivalent or superior to that of a prior art device comprising hole and electron injecting and transporting layers using an organic substance, possesses an extended life, weather resistance and high stability, and is inexpensive. This object is accomplished by the provision of an organic EL device which comprises a substrate, a hole injecting electrode and a cathode formed on the substrate, and an organic substance-containing light emitting layer located at least between these electrodes, wherein an inorganic insulating electron injecting and transporting layer is located between the light emitting layer and the cathode, and an inorganic insulating hole injecting and transporting layer is located between the light emitting layer and the hole injecting electrode. The inorganic insulating electron injecting and transporting layer comprises as a main component one or two or more oxides selected from the group consisting of strontium oxide, magnesium oxide, calcium oxide, lithium oxide, rubidium oxide, potassium oxide, sodium oxide and cesium oxide, and the inorganic insulating hole injecting and transporting layer comprises as a main component an oxide of silicon and / or an oxide of germanium. The main component has an average composition represented by (Si1-xGex) Oy where 0< / =x< / =1, and 1.7< / =y< / =1.99. The light emitting layer comprises a layer made up of a host substance on a side thereof contiguous to the inorganic insulating electron injecting and transporting layer and / or the inorganic insulating hole injecting and transporting layer. A layer containing a dopant in addition to the host substance is located on the side of the light emitting layer that faces away from the layer made up of the host substance or between them.

An O2-bearing low-Ce RE material with high performance and multiple purposes is a composite oxide consisting of cerium oxide, zirconium oxide and assistant chosen from lanthanum oxide, strontium oxide and yttrium oxide. It is prepared through codeposition and calcining at 500-600 deg.C. It can be used as the carrier and assistant of the catalyst for cleaning the tail gas of car.

The invention discloses a preparation method of iron strontium oxide magnetic nanoparticles and a magnetic damping rubber thereof, which solves the problem that the existing magnetic damping rubber fails to meet the requirements for excellent physical-mechanical properties and good magnetic damping effect simultaneously. In the preparation method of the iron strontium oxide magnetic nanoparticles, a chemical coprecipitation method is organically combined with a molten salt method to obtain surface-modified nano-grade iron strontium oxide in a regular shape, and then the obtained iron strontium oxide is used for preparing the magnetic damping rubber. The invention has the following advantages: the magnetic particles have nano-scale particle size and excellent magnetic property, and can be uniformly dispersed in a rubber matrix; a nitrile-butadiene rubber is taken as the matrix, thus having excellent oil resistance; and the magnetic damping rubber has excellent mechanical property.

An object of the invention is to achieve an organic EL device which has an extended life, weather resistance, high stability, and high efficiency, and is inexpensive as well. This object is accomplished by the provision of an organic EL device comprising a substrate, a pair of a hole injecting electrode and a cathode formed on the substrate, and an organic layer located between these electrodes and taking part in at least a light emission function, wherein between the organic layer and the cathode there is provided an inorganic insulating electron injecting and transporting layer comprising a first component comprising at least one oxide selected from the group consisting of lithium oxide, rubidium oxide, potassium oxide, sodium oxide and cesium oxide, a second component comprising at least one oxide selected from the group consisting of strontium oxide, magnesium oxide and calcium oxide, and a third component comprising silicon oxide and / or germanium oxide.

Provided are an amorphous polyamide resin composition having high transparency, and is excellent in heat resistance and stiffness, and a molded product thereof. The glass filler contains, expressed in terms of oxides by mass %, 68 to 74% of silicon dioxide (SiO2), to 5% of aluminum oxide (Al2O3), 2 to 5% of boron oxide (B2O3), 2 to 10% of calcium oxide (CaO), 0 to 5% of zinc oxide (ZnO), 0 to 5% of strontium oxide (SrO), 0 to 1% of barium oxide (BaO), 1 to 5% of magnesium oxide (MgO), 0 to 5% of lithium oxide (Li2O), 5 to 12% of sodium oxide (Na2O), and 0 to 10% of potassium oxide (K2O), where a total amount of lithium oxide (Li2O), sodium oxide (Na2O), and potassium oxide (K2O) is 8 to 12%.

A glass-ceramic composition contains first ceramic particles principally containing forsterite; second ceramic particles principally containing at least one selected from the group consisting of calcium titanate, strontium titanate, and titanium oxide; and borosilicate glass particles containing about 3% to 15% lithium oxide, about 20% to 50% magnesium oxide, about 15% to 30% boron oxide, about 10% to 45% silicon oxide, about 6% to 20% zinc oxide, 0% to about 15% aluminum oxide, and at least one additive selected from the group consisting of calcium oxide, barium oxide, and strontium oxide on a weight basis. The content of the borosilicate glass particles is about 3% or more; the lower limit of the content of the additive is about 2%; and the upper limit of the additive content is about 15%, about 25%, or about 25% when the additive is calcium oxide, barium oxide, or strontium oxide, respectively, on a weight basis.

The invention provides an organic EL device comprising a substrate, a hole injecting electrode and a negative electrode formed on the substrate, an organic layer containing an organic material between the electrodes, the organic layer including a light emitting layer having at least a light emitting function, and an electron injecting and transporting layer containing an electron transporting organic material and an inorganic insulative electron injecting and transporting layer formed of an inorganic material between the negative electrode and the light emitting layer. The inorganic insulative electron injecting and transporting layer contains at least one oxide selected from the group consisting of lithium oxide, rubidium oxide, potassium oxide, sodium oxide, cesium oxide, strontium oxide, magnesium oxide, and calcium oxide as a main component, and silicon oxide, germanium oxide or a mixture of silicon oxide and germanium oxide as a stabilizer. This construction ensures better performance than prior art devices having electron injecting and transporting layers using organic materials, a high efficiency, long life, weather resistance, and high stability.

The present invention belongs to the field of automobile tail gas purifying technology, and is especially glass ceramic coating on metal or alloy carrier of automobile tail gas purifying treater and its preparation process. The oxides of the glass coating include silica in 25-65 wt% and boron oxide in 5.0-27 wt%, except the mixture of other 3-9 oxides selected from 17 kinds of oxides, including sodium oxide, potassium oxide, lithium oxide, aluminum oxide, calcium oxide, etc. The glass coating on the metal carrier can raise the mechanical strength and reaction activity of the catalyst effectively, and this results in saving in active component and lowered cost.

The invention relates to an alkali-free aluminoborosilicate glass having a coefficient of thermal expansion alpha20 / 300 of between 2.8.10-6 / K and 3.6.10-6 / K, which has the following composition (in % by weight, based on oxide): silicon dioxide (SiO2)>58-65, boric oxide (B2O3)>6-11.5, aluminum oxide (Al2O3)>20-25, magnesium oxide (MgO) 4-<6.5, calcium oxide (CaO)>4.5-8, strontium oxide (SrO) 0-<4, barium oxide (BaO) 0.5-<5, with strontium oxide (SrO)+barium oxide (BaO)>3, zinc oxide (ZnO) 0-<2, and which is highly suitable for use as a substrate glass both in display technology and in thin-film photovoltaics.

To provide a process for producing and alkali free glass for effectively suppressing bubbles, and an alkali free glass produced by the process, which is suitable as a glass substrate for flat panel displays and has few bubbles.A process for producing an alkali free glass containing substantially no alkali metal oxide, which comprises melting a glass starting material having a matrix composition of the following composition, and subjecting the molten glass to a treatment process of removing bubbles under reduced pressure, stirring or transferring under a condition where the molten glass is in contact with a platinum member, wherein the starting material is prepared so as to contain SnO2 in an amount of from 0.01 to 2.0% per 100% of the total amount of the above matrix composition; the starting material is melted under heating at from 1,500 to 1,650° C.; then bubbles contained in the molten glass are permitted to rise to the surface of the molten glass, together with oxygen bubbles generated by a reduction reaction in which SnO2 in the molten glass is reduced to SnO; and in the above treatment process, the oxygen bubbles generated at the interface between the molten glass and the platinum member are permitted to be absorbed by an oxidation reaction in which SnO is oxidized to SnO2, under a condition where the molten glass is from 1,300 to 1,500° C.Composition as represented by the mass percentage:SiO258.4 to 66.0%,Al2O315.3 to 22.0%,B2O3 5.0 to 12.0%,MgO  0 to 6.5%,CaO  0 to 7.0%,SrO  4 to 12.5%,BaO  0 to 2.0%,MgO + CaO + SrO + BaO 9.0 to 18.0%.

The present invention provides one kind of supported calcium oxide catalyst and its preparation process and usage in preparing biological diesel oil. The supported calcium oxide catalyst has the co-catalyst of strontium oxide, zinc oxide or lanthanum oxide, carrier of magnesia, silica, alumina or magnesia-alumina, calcium oxide supporting amount of 2-30 wt% of the carrier and co-catalyst supporting amount of 0-16 wt% of the carrier. The supported calcium oxide catalyst has simple preparation process, high repeatability, high reaction activity for preparing biological diesel oil, insolubility in methanol system and easy separation from the reaction system.

An LED lamp includes a light source configured to emit radiation with a peak intensity at a wavelength between about 250 nm and about 550 nm; and a phosphor composition configured to be radiationally coupled to the light source. The phosphor composition includes particles of a phosphor of formula I, said particles having a coating composition disposed on surfaces thereof;((Sr1−zMz)1−(x+w)AwCex)3(Al1−ySiy)O4+y+3(x−w)F1−y−3(x−w)  Iwherein the coating composition comprises a material selected from aluminum oxide, magnesium oxide, calcium oxide, barium oxide, strontium oxide, zinc oxide, aluminum hydroxide, magnesium hydroxide, calcium hydroxide, barium hydroxide, strontium hydroxide, zinc hydroxide, aluminum phosphate, magnesium phosphate, calcium phosphate, barium phosphate, strontium phosphate, and combinations thereof; andA is Li, Na, K, or Rb, or a combination thereof;M is Ca, Ba, Mg, Zn, or a combination thereof; and0<x≦0.10, 0≦y≦0.5, 0≦z≦0.5, 0≦x≦x.

The invention provides a non-crystalline polyamide resin composition with enough transparency and excellent rigidity, mechanical performance, physical performance and heat resistance, and a product thereof. The composition adopts glass filler which is represented by the mass percentage based on oxide, contains 68-72 percent of silicon dioxide (SiO2), 2-5 percent of aluminum oxide (Al2O3), 2-5 percent of boron oxide (B2O3), 2-10 percent of calcium oxide (CaO), 0-5 percent of zinc oxide (ZnO), 0-5 percent of strontium oxide (SrO), 0-1 percent of barium oxide (BaO), 1-5 percent of magnesium oxide (MgO), 0-5 percent of lithium oxide (Li2O), 5-12 percent of sodium oxide (Na2O) and 0-10 percent of potassium oxide (K2O), wherein the total amount of lithium oxide, sodium oxide and potassium oxideis 8-12 percent.

The invention discloses a catalyst for preparing alcohol through hydrogenation of acetic acid, and a preparation method of the catalyst. The catalyst is a multicomponent load catalyst and comprises ingredients a, b and c, and a carrier, wherein the ingredient a is one or more of calcium, potassium, sodium, barium, strontium, calcium oxide, potassium oxide, sodium oxide, barium oxide and strontium oxide; the ingredient b is one or more of tin, cobalt, molybdenum, nickel, iron, tin oxide, cobalt oxide, molybdenum oxide, nickel oxide and iron oxide; the ingredient c is one of platinum, palladium, ruthenium, rhodium, platinum oxide, palladium oxide, ruthenium oxide and rhodium oxide; the carrier is silicon dioxide, cerium dioxide, titanium dioxide, graphite, aluminum oxide or active carbon; and the mass ratio of the ingredient a to the ingredient b to the ingredient c to the carrier is (1-20):(0.5-2):(0.5-1):100. The multicomponent load catalyst is prepared by a multistep impregnation method, and used for preparing alcohol through the hydrogenation of acetic acid, and results prove that the catalyst is excellent in catalytical performance, long in service life and high in reaction stability.

An aqueous coating composition comprises a metal oxide selected from the group consisting of bismuth oxide, vanadium oxide, manganese oxide, cobalt oxide, zinc oxide, strontium oxide, yttrium oxide, molybdenum oxide, zirconium oxide, lanthanum oxide, oxides of the lanthanide series of elements and combinations thereof and an electrodepositable binder, the binder comprising (a) a phosphorous-containing groupin which X is a hydrogen, a monovalent hydrocarbon, an alkyl group such as an aminoalkyl group, or an oxygen atom having a single covalent bond to the phosphorous atom, and each oxygen atom has a covalent bond to a hydrogen atom, an alkyl group, an aryl group, an alkylaryl group, an arylalkyl group, or the resin, with the caveat that at least one oxygen atom has a covalent bond to resin; (b) a carboxylate group separated by from 2 to 4 carbons from an ester group; and (c) a tridentate amine ligand. The coating composition can be electrodeposited on a metal substrate to provide superior corrosion resistance.

The present invention relates to one kind of far infrared magnetic fiber and its production process, and features that the base material for producing the far infrared magnetic fiber is dacron, polypropylene or nylon with mixed superfine powder of ferric oxide, barium oxide, strontia, silica, calcium oxide and manganese oxide, accounting for 2-8 wt%. The production process of the far infrared magnetic fiber includes the steps of: preparing the mixed superfine powder, mixing the mixed superfine powder, the polymer slicing and assistant through smelting and stirring, pelletizing the mixture in a double screw pelletizing machine to form agglomerate, heating the agglomerate to form melt, extruding with a screw extruder and a metering pump through a orifice, condensating and curing, and stretching to form far infrared magnetic fiber.

The invention provides an unleaded glass powder used for electronic paste and a preparation method thereof. The unleaded glass powder is composed of the following components by mass ratio: 10-60% of diboron trioxide, 2.5-30% of silicon dioxide, 30-75% of bismuth trioxide, 0.1-5% of sodium oxide, 0.1-3% of calcium oxide, 0.5-10% of strontium oxide, 1.5-20% of titanium dioxide, 0.5-8% of zirconium oxide, 0.1-5% of stannic oxide, 0.5-6% of aluminium oxide, 0.5-5% of antimonous oxide and 0.1-5% of calcium fluoride, the components are fully mixed to be uniform and then heated to 1050-1250 DEG C, and heat preservation is carried out for 30-120min, so that raw material is fully melted into glass metal, the glass metal is poured into deionized water to be quenched into glass granules, and ball milling into 320-400 meshes is carried out, thus obtaining the unleaded glass powder. The invention provides an unleaded glass powder with low softening temperature, good chemical stability, appropriate expansion coefficient, acid-base resistance, good abrasive resistance, wide sintering temperature range, low manufacturing cost and no toxic heavy metal oxide, and the unleaded glass powder has wide application range.

The invention relates to medical titanium with a trace element slow-release function or a titanium alloy implant material as well as a preparation method and an application of the medical titanium. The invention adopts the technical scheme that the preparation method comprises the following steps: putting a polished titanium-containing metal sheet into an electrolyte as an anode for anodic oxidation; flushing and drying the titanium-containing metal sheet subjected to anodic oxidation, carrying out heat treatment for 1-3 hours at a temperature of 100-500 DEG C, naturally cooling and ultrasonically cleaning and drying; and putting the dried titanium-containing metal sheet into one of or mixed solution of more than any two strontium hydroxide, strontium acetate, zinc acetate or magnesium acetate, carrying out hydrothermal reaction for 0.5-12 hours in a closed container at a temperature of 100-300 DEG C, naturally cooling, taking out, cleaning and drying, and carrying out heat treatment for 1-3 hours at a temperature of 450-550 DEG C to obtain the medical titanium with the trace element slow-release function or the titanium alloy implant material. The medical titanium or the titanium alloy implant material as well as the preparation method and the application thereof have the beneficial effects that the preparation method is simple and reliable, the loading quantity and the release amount of trace elements of the medical titanium in a nano tube are controllable, the medical titanium and the biological activity on the alloy surface can be better promoted, and the application prospect is good in the medical implant material.

The invention aims at providing a heat-corrosion-resistant composite enamel coating and a preparation method thereof. The heat-corrosion-resistant composite enamel coating is characterized by comprising an enamel matrix and ceramic particles, wherein the ceramic particles are corundum with the size of less than 5 mum, and the addition amount of the ceramic particles accounts for 15-30 wt% of the weight of the composite enamel coating; and the enamel matrix comprises the following components: 58-62 wt% of silicon dioxide, 10-13 wt% of zirconia dioxide, 5-8 wt% of aluminum oxide, 5-7 wt% of calcium oxide, 4-6 wt% of diboron trioxide, 2-4 wt% of strontium oxide, 2-4 wt% of titanium dioxide, 2-6 wt% of sodium oxide and / or potassium oxide and 0-2 wt% of nickel oxide. The heat-corrosion-resistant composite enamel coating has no problems of continuous dissolving of an alloy matrix caused by easy occurrence of excessive interface reaction between the conventional enamel coating and high temperature alloy matrix during high temperature service, and overhigh content of low-melting-point components and poor diffusion infiltration resistance of the conventional enamel coating, and has excellent comprehensive resistance against heat corrosion and thermal circulation spalling.

The invention discloses a high-catalytic-activity amorphous metal oxide hydrogen evolution electrode and a preparation method thereof. The electrode comprises an active coating made from an amorphous metal oxide, which is selected from any one or more of amorphous nickel oxide, amorphous ruthenium oxide, amorphous molybdenum oxide, amorphous cerium oxide, and amorphous strontium oxide. The preparation method comprises: step1, pre-treating a nickel screen to form a porous transition nickel oxide layer; step2, preparing an active coating precursor solution and coating the nickel screen with the precursor solution; and step3, performing thermal decomposition and laser-cladding assisted solidification to obtain the hydrogen evolution electrode. The preparation method is simple and is low in thermal decomposition temperature. The prepared hydrogen evolution electrode is high in catalytic activity and is not prone to polarize in a high current density. A catalyst firmly combines with a matrix and is not prone to fall off. The hydrogen evolution electrode has excellent anti-reverse-current performance. Compared with a conventional nickel screen, in a high current density of 4000A / m<2>, the electrode can reduce the hydrogen evolution overpotential by 250 mV. In a situation of frequent startup and shutdown, the voltage of an electrolytic bath is stable, and the fluctuation amplitude is small.

The invention provides ultraviolet-radiation-resistant optical glass high in ultraviolet band transmittance. The optical glass is prepared from, by weight, 60-70 parts of phosphoric acid, 13-15 parts of boric acid, 8-12 parts of aluminum oxide, 4-6 parts of barium carbonate, 4-6 parts of potassium carbonate, 3-5 parts of calcium carbonate, 1-1.8 parts of a coloring agent A, 2-2.8 parts of a coloring agent B, 0.5-1 part of a reducing agent and 0.5-1 part of a stabilizing agent, wherein the stabilizing agent is composed of cerium oxide and strontium oxide, a ratio of strontium oxide to cerium oxide is 2:1, the coloring agent A refers to cobalt oxide, the coloring agent B refers to nickel oxide, a ratio of nickel oxide to cobalt oxide is 1:2, and tartaric acid serves as the reducing agent. The optical glass has advantages that a great ultraviolet radiation resistance function of the ultraviolet glass is achieved while ultraviolet band transmittance of the ultraviolet glass is increased, and the technical problem that the peak transmittance, which is required to be 85% or above in practical application, of current ultraviolet glass at an ultraviolet band is only about 80% is solved.

Performance of an electronic device is highly improved by epitaxially growing a perovskite-type oxide thin film on an inorganic amorphous layer or an organic solid layer in a desired direction; and furthermore, a high performance electronic device is provided by incorporating the electronic device into an integrated circuit, wherein oxide thin layers are formed on the inorganic amorphous layer or the organic solid layer, and the perovskite-type oxide thin film is grown epitaxially on the oxide layer, the oxide thin layers being able to be at least one of strontium oxide, magnesium oxide, cerium oxide, zirconium oxide, yttrium stabilized zirconium oxide, and strontium titanate; and as the perovskite-type oxide thin film, the perovskite-type oxide thin film being a piezoelectric or ferroelectric material, for example, is used.