11101 results about "Titanate" patented technology

A structure for use in high temperature applications and including a porous ceramic material consisting essentially of about 50-90 percent by weight iron or magnesium stabilized aluminum titanate (AlTiO5) and about 10-50 percent by weight strontium feldspar (SrO.Al2O3.2SiO2), and having a coefficient of thermal expansion over a temperature range from room temperature to 1000° C. of about -10x10-7/° C. to +15x10-7/° C., a heat capacity at 500° C. greater than 3.2 J/cm3K, a porosity of about 15-50 percent by volume, preferably 40-50 percent by volume, and a median pore size of about 5-50 micrometers, preferably 8-15 micrometers. The structure is especially useful as a diesel exhaust particulate filter.

A ceramic forming batch mixture including inorganic batch materials, such as sources of alumina, titania, and silica, a pore former combination including first and second pore formers with different compositions; an organic binder; and a solvent. Also disclosed is a method for producing a ceramic article involving mixing the inorganic batch materials with the pore former combination having first and second pore formers of different composition, adding an organic binder and a solvent, forming a green body; and firing the green body. A green body having a combination of first and second pore formers with different compositions is disclosed, as are several methods for firing to produce ceramic articles such as aluminum titanate.

In one embodiment, the invention is a process for the preparation of poly(trimethylene terephthalate) comprising (a) contacting terephthalic acid with 1,3-propanediol in the presence of an organic tin catalyst to form a bis(3-hydroxypropyl)terephthalate monomer; and (b) polymerizing said monomer in the presence of organic titanate polycondensation catalyst to obtain the poly(trimethylene terephthalate). In another embodiment, the invention is a process for the preparation of poly(trimethylene terephthalate) containing less than 1.6 mol % of DPG said process comprising contacting terephthalic acid with a 1.6 to 1 to 2:1 molar amount of 1,3-propanediol in the presence of 20 to 120 ppm (as tin), by weight of the poly(trimethylene terephthalate), of a organic tin catalyst, to form a bis(3-hydroxypropyl)terephthalate monomer and polymerizing said monomer to obtain the poly(trimethylene terephthalate). The invention is also directed to poly(trimethylene terephthalate) produced by the processes.

A porous ceramic honeycomb filter manufactured from an oxide-based ceramic material having a pore size distribution with d₁≧7.0 microns. Preferably, the oxide-based material is cordierite or aluminum titanate. Alternatively, the filter contains a cordierite-containing ceramic body with a narrow pore size distribution with d_b≦1.00, wherein d_b=(d₉₀−d₁₀)/d₅₀. Also disclosed is a batch mixture, method and honeycomb green body made from mixture of inorganic source materials selected from the group of magnesia sources, alumina sources, and silica sources, and a pore former having a narrow particle size distribution with d_ps≦0.90, wherein d_ps={(dp₉₀−dp₁₀)/dp₅₀}. The pore former is preferably selected from a group consisting of canna starch, sago palm starch, green mung bean starch, and single-mode potato starch.

The invention is directed at a mullite-aluminum titanate porous diesel particulate filter constituting a porous ceramic body containing, expressed in terms of weight percent of the total body, of 60-90%, preferably 70-80%, most preferably 70% iron-aluminum titanate solid solution having a stoichiometry of Al2(1-x)Fe2xTiO5, where x is 0-0.1, and 10-40%, preferably 20-30%, most preferably 30% mullite (3Al2O3.2SiO2), and consists essentially, expressed in terms of weigh percent on the oxide basis, of 3 to 15% SiO2, 55 to 65% Al2O3, 22 to 40% TiO2, and 0 to 10% Fe2O3, and being useful for filtration of diesel exhaust. The inventive diesel particulate filter exhibits high interconnected open porosity and large median pore size, in combination with high permeability when fired to a temperature of between 1650° to 1700° C., along with high thermal shock resistance and good filtration capability.

An aluminum titanate-based ceramic article having a composition comprising u (Al₂O₃—TiO₂)+v (R)+w (3Al₂O₃—2SiO₂)+x (Al₂O₃)+y (SiO₂)+z (1.1SrO-1.5Al₂O₃-13.6SiO₂—TiO₂)+a (Fe₂O₃—TiO₂)+b (MgO-2TiO₂), where, R is SrO—Al₂O₃-2SiO₂ or 11.2SrO-10.9Al₂O₃-24.1SiO₂—TiO₂, where u, v, w, x, y, z, a and b are weight fractions of each component such that (u+v+w+x+y+z+a+b=1), and 0.5<u≦0.95, 0.01<v≦0.5, 0.01<w≦0.5, 0≦x≦0.5, 0≦y≦0.1, 0≦z≦0.5, 0<a≦0.3, and 0≦b≦0.3. A method of forming the ceramic article is provided. The ceramic article is useful in automotive emissions control systems, such as diesel exhaust filtration.

The invention relates to zeolite-based composite antibiotic material and a process for preparation, the material of which is low-silicon-aluminum-ratio zeolite molecular sieve which is used as the base and carrier, the outer surface of the invention is covered with nanometer titanium dioxide particles, and the pore passages or cages of the invention are provided with metallic ions which have antibiotic effect. The process for preparing the material is that low-silicon-aluminum-ratio zeolite molecular sieve absorbs organic amine to saturation and then is dipped into soluble titanates for roasting to generate nanometer titanium dioxide on the outer surface of zeolite, and metallic ions such as silver ions, copper ions and the like which have antibiotic effect are exchanged to zeolite by the ion exchange process to form the novel composite antibiotic material. The composite antibiotic material not only has the antibiotic effect of metallic ions but also has the antibiotic effect of nanometer titanium dioxide, and thereby the antibiotic effect is strengthened. The composite antibiotic material is easy to prepare, low in price and suitable for industrial production.

A core composition of a metal-cored wire comprising a combination of graphite and potassium compounds has been proven to stabilize the arc in a straight polarity welding configuration. In particular, adding a combination of graphite and potassium manganese titanate (K₂MnTiO₄) and potassium sulfate (K₂SO₄) in the preferred combination of graphite and potassium compounds from the range of about 0.3% to about 5.0% wt resulted in a greatly stabilized arc, reduced spatter and reduced warpage while maintaining high deposition rates of the DCEN welding process

The invention belongs to the field of environmental protection and environmental catalysis, and in particular relates to a novel composite carrier SCR flue gas denitration catalyst. An SCR flue gas denitration catalyst which takes TiO2-mesoporous SiO2 as a compound carrier is obtained by preparing the TiO2-mesoporous SiO2 by hydrolyzing tetrabutyl titanate in mesoporous SiO2 by adopting a sol-gel method, taking the TiO2-mesoporous SiO2 as the compound carrier of the SCR catalyst, supporting a cocatalyst on the TiO2-mesoporous SiO2 compound carrier, and finishing the supporting of a main catalyst. The catalyst comprises the following components in percentage by mass: 85 to 99.9 percent of the compound carrier, 0 to 5 percent of the cocatalyst and 0.1 t0 10 percent of the main catalyst, wherein the compound carrier consists 80 to 95 weight percent of the mesoporous SiO2 and 5 to 20 weight percent of the TiO2. The introduction of the mesoporous SiO2 greatly increases the specific area of the catalyst; and the catalyst has high dispersibility of active substance and high stability, contributes to a gas to enter pores to fully react with the catalyst because the carrier has regular pore structures, and has high denitration performance.

A non-asbestos friction material includes at least one binder, fiber, lubricant, abrasive and titanate in a range of volume fractions in combination with other materials such as fillers and is substantially free of copper and asbestos.

The invention relates to a preparation method of an SCR denitration catalyst, which comprises the following steps: (1) Al2O3 sol is prepared, which comprises the steps that hot ammonia, the Al2O3 is added in drops into the ammonia and then HCI is added and the mixture is stirred; (2) Al2O3-SiO2-TiO2 composite sol is prepared, which comprises the steps that tetratethoxy-silane, butyl titanate, deionized water are sequentially put into ethanol to be aging and then the sol prepared by step (1) is adding to be stirred and aging; (3) vector is coated, which comprises the steps that cordierite honeycomb immersed into the sol of step (2) and the raffinate in a channel is cleaned, dried and roasted after being taken out; (4) active component impregnating solution is prepared, which comprises the steps that lanthanum nitrate, ammonium metavanadate and ammonium paratungstate are dissolved into the deionized water after being mixed together and oxalate acid is added to be aging; (5) the active component is loaded, which comprises the steps that the vector of the step (3) is immersed into the impregnating solution of the step (4) and then the raffinate in the channel is cleaned to be dried and roasted. The invention also relates to the denitration catalyst which is prepared by the method.

The invention relates to a natural super-hydrophilic porous TiO2/SiO2 composite thin film and a preparation method thereof. The preparation method comprises the following steps of: adopting a sol-gel method and respectively taking tetrabutyl titanate and ethyl orthosilicate as precursors to prepare TiO2 sol and SiO2 sol; calculating according to the molar fraction, compounding through taking the addition quantity of the SiO2 sol as 1-50 percent of total contents of SiO2 and TiO2 to obtain TiO2/SiO2 composite sol; and coating the prepared composite sol on a substrate material, airing, calcining and cooling to obtain the super-hydrophilic thin film. The natural super-hydrophilic porous TiO2/SiO2 composite thin film and the preparation method thereof have the beneficial effects that the thin film prepared by the method has the double effects of phase separation-induced developed hole structure and SiO2 compounding, the aperture of the thin film is within the scope of 100 nm-6 mum, the thickness of the thin film is within the scope of 200 nm-20 mum, a contact angle of the surface of the thin film with water is below 5 degrees, and the self-cleaning, antifogging and antibacterial functions are optimal.

The invention provides a method for preparing a small-crystallite titanium-silicon molecular sieve in a cheap system by changing the adding mode of seed crystals and by a hydrothermal process. The titanium-silicon molecular sieve is prepared by using silicon sol as a silicon source, titanium tetrachloride or tetrabutyl titanate as a titanium source, tetrapropylammonium bromide ( TPABr) as a template agent, organic amine as an alkali source and unseparated nanoscale TS-1 mother liquor as seed crystals directly and by the hydrothermal process. The grain size of the titanium-silicon molecular sieve is less than 1 micrometer, and the titanium-silicon molecular sieve has high activity for selective oxidization reactions using hydrogen peroxide as an oxidant, such as epoxidation of olefins, hydroxylation of phenol, ammoxidation of cyclohexanone and the like. The method simplifies the synthesis process of small crystallite TS-1 in the cheap system and reduces synthesis time and cost.

Environmental barrier coatings for high temperature ceramic components including: a bond coat layer; an optional silica layer; and at least one transition layer including: from about 85% to about 100% by volume of the transition layer of a primary transition material selected from a rare earth disilicate, or a doped rare earth disilicate; and from 0% to about 15% by volume of the transition layer of a secondary material selected from Fe₂O₃, iron silicates, rare earth iron oxides, Al₂O₃, mullite, rare earth aluminates, rare earth aluminosilicates, TiO₂, rare earth titanates, Ga₂O₃, rare earth gallates, NiO, nickel silicates, rare earth nickel oxides, Lnb metals, Lnb₂O₃, Lnb₂Si₂O₇, Lnb₂SiO₅, borosilicate glass, alkaline earth silicates, alkaline earth rare earth oxides, alkaline earth rare earth silicates, and mixtures thereof; where the transition layer is applied to the component as a slurry including at least water, the primary transition material and at least one slurry sintering aid, and where a reaction between the slurry sintering aid and the primary transition material results in the transition layer having a porosity of from 0% to about 15% by volume of the transition layer.

In order to degrade the pollutants in water and atmosphere by the photocatalysis technology, the invention discloses a method for preparing a high activity non-metallic ion co-doped titanium dioxide photochemical catalyst. In the photochemical catalyst, titanium ester or titanate is used as a precursor, non-metallic compound comprising boron, carbon, nitrogen, fluorin, silicon, phosphor, sulfur, chlorine, bromine, iodine, and the like, are used as doping agents, the high activity non-metallic ion co-doped titanium dioxide photochemical catalyst is prepared by adopting the sol gel method. Compared with a titanium dioxide photochemical catalyst single-doped with pure titanium dioxide and the non-metallic irons, the visible light catalytic activity of the titanium dioxide photochemical catalyst on the degradation of parachlorophenol is greatly improved, and the ultraviolet light catalytic activity can also exceed the catalytic activity of the pure titanium dioxide catalyst. The method also has the advantages that the preparation technique is simple, the equipment requirement is low; the particle diameter of the product is small, the specific surface is relatively high, the dispersivity is good, thus having a wide application prospect in the environmental cleaning scientific field.

A sintered rod-shaped proppant and anti-flowback agent possesses high strength and high conductivity. The sintered rods comprise between about 0.2% by weight and about 4% by weight aluminum titanate. In some embodiments, the sintered rods are made by mixing bauxitic and non-bauxitic sources of alumina that may also contain several so-called impurities (such as TiO₂), extruding the mixture, and sintering it. The starting material may optionally be milled to achieve better compacity and crush resistance in the final sintered rod. A fracturing fluid may comprise the sintered rods alone or in combination with a proppant, preferably a proppant of a different shape.

Nanomaterials of the JT phase of the titanium oxide TiO_2-x, where 0≦x≦1 having as a building block a crystalline structure with an orthorhombic symmetry and described by at least one of the space groups 59 Pmmn, 63 Amma, 71 Immm or 63 Bmmb. These nanomaterials are in the form of nanofibers, nanowires, nanorods, nanoscrolls and/or nanotubes. The nanomaterials are obtained from a hydrogen titanate and/or a mixed sodium and hydrogen titanate precursor compound that is isostructural to the JT crystalline structure. The titanates are the hydrogenated, the protonated, the hydrated and/or the alkalinized phases of the JT crystalline phase that are obtained from titanium compounds such as titanium oxide with an anatase crystalline structure, amorphous titanium oxide, and titanium oxide with a rutile crystalline structure, and/or directly from the rutile mineral and/or from ilmenite. The titanates are submitted to dynamic thermal treatment in an inert, oxidizing or reducing atmosphere to produce the JT phase of the TiO_2-x, where 0≦x≦1 with an orthorhombic structure.

A process for preparing the nanometre tubes of hydrated sodium titanate and titanate series includes such steps as hydrothermal reaction of TiO2 or metatitanic acid to obtain the nanometre tubes of hydrated sodium titanate, mixing them with the solution containing one or two kinds of metal ions to convert them to the nanometre tubes of hydrated titanate or composite hydrated titanates of the saidmetal ions, and thermal dewatering to obtain the nanometre tubes of corresponding titanate or composite titanates. Its advantages are uniform shape, large specific surface area, high thermal stability and regulatable catalytic performance.

The invention relates to the field of aluminum alloy decoration and protection coating for ships, in particular relates to an environmentally-friendly corrosion-contamination resistant chemical conversion agent and application thereof in a chromium-free chemical conversion film, and solves the problems of poor corrosion resistance, high cost, difficulty in large-area construction and the like in the prior art. The chemical conversion agent comprises a component A and a component B. The method for preparing a chemical conversion film comprises the following steps of: forming a first inorganic chemical conversion film layer by the component A and forming an organic contamination resistant closed film by the component B. The component A is a water solution prepared from a main salt, a film-forming accelerator, a buffering agent, a surfactant and the like, and the component B is prepared from silicate, silane, a silica sol, titanate, zirconate, waterborne resins and the like. The chemicalconversion agent does not contain chromium ions and phosphates, and the chromium-free chemical conversion film prepared from the chemical conversion agent has excellent corrosion resistance and contamination resistance, can be used for construction of large-area aluminum alloy sections, and can be used as surface decoration and protection coatings for 5xxx and 6xxx series aluminum alloys.

The invention provides a high strength organic / inorganic nano composite film layer materials and method for preparation, wherein the composition comprises 10-13% of titanate, 7-17% of silicane coupling agent, 0-6% of silicate ester, 40-65% of alcohol solvent and 1-4% of water. The preparation of the composition consists of using inorganic acid as catalyst, co-hydrolyzing titanate, silicate and silane coupling agent in dimethyl carbinol, coating the obtained paint by rotary, dipping or spraying methods onto the surface of the appliances, finally solidifying 1-3 hours at 135- 150 deg. C.

The invention relates to a preparation method and application method of a titanium dioxide nanosheet supported MIL-100 (Fe) composite photocatalysis material, belongs to the field of titanium dioxide photocatalysis, and especially relates to the field of titanium dioxide nanosheet supported porous metal organic skeleton (MOFs) composite materials. The preparation method comprises the following steps: 1, uniformly stirring tetrabutyl titanate and hydrofluoric acid at normal temperature, putting the obtained mixture in a hydrothermal reaction kettle, carrying out a reaction, separating the obtained material, washing the separated material, and drying the washed material to obtain titanium dioxide nanosheets; and 2, uniformly dispersing the titanium dioxide nanosheets in an anhydrous ethanol solution of iron trichloride, carrying out magnetic stirring at normal temperature for 15 min, carrying out suction filtration separation to obtain a product, dispersing the product in an anhydrous ethanol solution of trimesic acid, carrying out a 50-80 DEG C water bath reaction for 20-50 min, carrying out suction filtration separation to obtain a product, and repeating above processes in step 2 2-50 times to obtain the titanium dioxide nanosheet supported MIL-100 (Fe) composite photocatalysis material. The catalyst prepared through the method is especially suitable for catalytic degradation of high-concentration organic dyes (such as methylene blue) under visible light irritation) to reach a very high degradation rate.