39657 results about "Titanium dioxide" patented technology

A catalyst for treating exhaust gas from an internal combustion engine includes a carrier body coated with an inner layer and an outer layer. The inner layer includes platinum deposited on a first support material and on a first oxygen storage component, and the outer layer includes platinum and rhodium deposited on a second support material and on a second oxygen storage component. The first and second support materials may be the same or different, and may be selected from the group of: silica, alumina, titania, zirconia, mixed oxides or mixtures thereof, and zirconia-rich zirconia/ceria mixed oxide. The first and second oxygen storage components may include ceria-rich ceria/zirconia mixed oxide compounds, optionally including praseodymia, yttria, neodymia, lanthana or mixtures thereof.

The invention provides a high selectivity catalyst used for catalyzing and completely oxidizing formaldehyde with low concentration at room temperature. The catalyst can catalyze formaldehyde completely so as to lead the formaldehyde to be converted into carbon dioxide and water at room temperature. In addition, the conversion rate of formaldehyde remains 100% within a long period of time, without complex auxiliary facilities such as light source, a heating oven and the like, and external conditions. The catalyst comprises three parts which are inorganic oxide carrier, noble metal component and auxiliary ingredient. Porous inorganic oxide carrier is one of cerium dioxide, zirconium dioxide, titanium dioxide, aluminium sesquioxide, tin dioxide, silicon dioxide, lanthanum sesquioxide, magnesium oxide and zinc oxide or the mixture thereof or composite oxide thereof, zeolite, sepiolite and porous carbon materials. The noble metal component of the catalyst is at least one of platinum, rhodium, palladium, gold and silver. The auxiliary ingredient is at least one of the alkali metals of lithium, sodium, kalium, rubidium and cesium. The loading of the noble metal component used in the catalyst of the invention is 0.1 to 10% according to weight converter of metal elements and the selective preference is 0.3 to 2%. The loading of the auxiliary ingredient is 0.2 to 30% according to weight converter of metal elements and the selective preference is 1 to 10%. When the loading of the auxiliary ingredient is lower than 0.2% or higher than 30%, the activity of the catalyst for catalyzing and oxidizing formaldehyde at room temperature is decreased remarkably.

Disclosed is a catalyst. The catalyst comprises palladium, gold, and a support comprising titanium dioxide and tungsten trioxide. The support preferably comprises from 75 wt % to 99 wt % of titanium dioxide and from 1 wt % to 25 wt % of tungsten trioxide. A method for preparing the catalyst is also disclosed. The method comprises impregnating the support with a palladium compound and a gold compound, calcining the impregnated support, and then reducing the calcined support. Further disclosed is a method for preparing vinyl acetate with the catalyst. The catalyst exhibits improved catalytic activity and selectivity.

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.

The invention provides a multifunctional composite absorbing material for purifying water and a preparation method thereof, relating to an absorbing material. The invention provides the multifunctional composite absorbing material for purifying water, which can be used for effectively removing a plurality of harmful substances in the water and has higher removal efficiency and lower production cost, and the preparation method thereof. The absorbing material is selected from at least one of absorbing materials A, B and C; the absorbing material A takes a mesoporous adsorption ceramic material as a carrier to load nano metals including nano silver, nano zinc, nano iron and nano cerium; the absorbing material B takes the mesoporous adsorption ceramic material as the carrier to load nano metal oxides including nano titanium dioxide, nano zinc oxide, nano ferric oxide and nano cerium dioxide; and the absorbing material C is prepared from the following raw materials according to the mass ratio: 100-200 parts of active carbon powder, 20-30 parts of polyethylene powder, 10-30 parts of calcium sulfite powder, 10-30 parts of natural zeolite powder, 20-40 parts of macroporous acrylic resin and 10-20 parts of attapulgite powder.

A photovoltaic (PV) structure is provided, along with a method for forming a PV structure with a conductive nanowire array electrode. The method comprises: forming a bottom electrode with conductive nanowires; forming a first semiconductor layer of a first dopant type (i.e., n-type) overlying the nanowires; forming a second semiconductor layer of a second dopant type, opposite of the first dopant type (i.e., p-type), overlying the first semiconductor layer; and, forming a top electrode overlying the second semiconductor layer. The first and second semiconductor layers can be a material such as a conductive polymer, a conjugated polymer with a fullerene derivative, and inorganic materials such as CdSe, CdS, Titania, or ZnO. The conductive nanowires can be a material such as IrO₂, In₂O₃, SnO₂, or indium tin oxide (ITO).

The invention discloses an odorless anti-formaldehyde environment-friendly internal wall latex paint and a preparation method thereof. The odorless anti-formaldehyde environment-friendly internal wall latex paint is prepared from the following components in percentage by weight: 1-15% of visible light induced nano titanium dioxide photocatalyst slurry, 15-35% of odorless emulsion, 1-15% of formaldehyde absorbent, 0.5-2% of dispersing agent, 0.2-3% of thickening agent, 0.2-1% of wetting agent, 0.1-1% of defoaming agent, 0.5-5% of film-forming assistant, 0.2-3% of anti-freeze agent, 20-40% of pigment and filler, 0.1-1% of pH regulator, 0.01-0.1% of anticorrosive bactericide and 15-40% of deionized water. The invention adopts an IPS+odorless technique, and the visible light induced nano titanium dioxide photocatalyst and the formaldehyde absorbent are added, thereby achieving the optimal effect of removing formaldehyde and other harmful substances through physical adsorption and chemical decomposition. The invention can be widely used for decorative spraying of various internal walls and other constructions.

Isopipes for use in making sheet glass by a fusion process are provided which exhibit reduced sag. The isopipes are composed of a zircon refractory which has a mean creep rate (MCR) at 1180° C. and 250 psi and a 95 percent confidence band (CB) for said mean creep rate such that the CB to MCR ratio is less than 0.5, the MCR and the CB both being determined using a power law model. The zircon refractory can contain titania (TiO₂) at a concentration greater than 0.2 wt. % and less than 0.4 wt. %. A concentration of titania in this range causes the zircon refractory to exhibit a lower mean creep rate than zircon refractories previously used to make isopipes. In addition, the variation in mean creep rate is also reduced which reduces the chances that the zircon refractory of a particular isopipe will have an abnormally high creep rate and thus exhibit unacceptable sag prematurely.

The invention relates to a method of preparing a solution containing colloidal particles which contain crystalline titanium dioxide wherein one or more hydrolysable titanium-containing compound(s) is stabilised by oxalic acid in a reaction medium. The reaction further relates to the preparation of titania materials (including particulate materials, coating solutions and films) which comprise or include anatase phase titania, and so are suitable in photocatalytic applications. The invention also deals with a method of preparing B-phase titania.

The invention relates to a preparation method of a graphene/titanium dioxide composite photocatalyst, which comprises the following steps: dissolving oxidized graphite in an organic solvent and obtaining oxidized graphene dispersion by ultrasonic processing; adding titanium salt precursor to the oxidized graphene dispersion and stirring evenly; transferring the mixed dispersion into a hydrothermal reaction kettle and reacting at 120-200 DEG C for 4-20 hours; respectively cleaning the product of the reaction by absolute ethyl alcohol and de-ionized water; and drying in vacuum at 40-80 DEG C for 8-24 hours to obtain the graphene/titanium dioxide composite photocatalyst. The invention has the advantages of common and easily obtained raw material, low cost and simple and safe preparation process, and in the obtained product, TiO2 particles can be evenly dispersed on the surface of the graphene, and stronger acting force is formed between the TiO2 particles and the surface of the graphene, thereby avoiding aggregation of the particles and effectively preventing restacking of graphene laminas. The graphene/titanium dioxide composite photocatalyst has good photocatalysis activity due to structural advantages and has potential application value in the fields of environment protection and solar cells.

The invention is directed to ultra-low expansion glasses to which adjustments have been made to selected variables in order to improve the properties of the glasses, and particularly to lower the expansivity of the glasses. The glasses are titania-doped silica glasses. The variables being adjusted include an adjustment in β-OH level; an adjustment to the cooling rate of the molten glass material through the setting point; and the addition of selected dopants to impact the CTE behavior.

A solid composite electrolyte membrane for use in a lithium battery is provided which exhibits a conductivity ranging from about 10⁻⁴ S cm⁻¹ to about 10⁻³ S cm⁻¹ at ambient temperature. The membrane is formed by providing a glass or glass-ceramic powder formed from a mixture of lithium carbonate, alumina, titanium dioxide, and ammonium dihydrogen phosphate. The powder is mixed with a conditioning agent and at least one solvent, followed by the addition of a binder and one or more plasticizers. The resulting slurry is cast into a tape which is then subjected to a binder burn-off and sintering process to form the membrane. The resulting membrane may be a glass-ceramic composite having a porosity ranging from 0 to 50%, or the membrane may be further infiltrated with a polymer to form a water-impermeable polymeric-ceramic composite membrane.

The invention discloses an electrode material of composite lithium titanate and its preparation method, which is secondary particles with spherical or similar spherical shape and porous nanometer channels, which is made from lithium titanate particles, nano-carbon coated materials and doped modifier. The preparation method includes: milling the inorganic lithium salt, titanium dioxide, nano-carbon coated material or doped modifier, scattering them into the organic solvent for further drying, processing heat treatment, and cooling. Comparing with the existing technologies, this electrode material has the high-rate performance, highly reversible electrochemical capacity, and smaller surface area to enhance its first Coulomb efficiency and cycle stability, applying to rechargeable and once-use lithium-ion battery.

A protective coating for a substrate is disclosed having an outer component or module formed of a swellable material and an inner module formed of a plurality of layer or bilayers formed of ceramic material. The coating comprising a plurality of modules comprising a first module comprising a number (m) of bilayers comprising zirconia and alumina wherein (m) is a number greater than 1. The coating further comprises a second module disposed on the first module comprising a number (n) of bilayers comprising zirconia and titania wherein (n) is a number greater than 1. The coating further comprises a third module disposed on the second module comprising a third-module compound capable of forming a hydrate or hydroxide compound upon contact with an oxygen containing environment.

Provided is a waterborne ultra-thin steel structure fire retardant coating and a preparation method thereof. The raw material ratio of the coating includes 15-50% by weight of polymer latex, 15-30% by weight of ammonium polyphosphate, 5-15% by weight of pentaerythritol, 3-10% by weight of cyanurtriamide, 5-12% by weight of titanium dioxide, 2-13% inorganic filler, 0-5% by weight of expansiveness graphite, 1-10% by weight of plasticizer, 0.4-1.5% by weight of wetting dispersant, 0.2-0.5% by weight of defoamer, 1-6% by weight of coalescing agents and 5-15% by weight of water, and total raw material ratio is 100%. A high-speed dispersion method or a grinding dispersion method is adopted in preparation of the coating. A coating layer of the fire retardant coating can form a carbonization layer which is good in foaming effect, small and uniform in air holes and high in expansion times when in heating. The final fire retardant performance of the coating is far higher than technical requirements of a national standard. The waterborne ultra-thin steel structure fire retardant coating is a waterborne coating product, is non-poisonous and odorless and environment-friendly, and can be coated in a mode of brushing or spraying or roller coating.

The invention discloses recovery process of honeycomb type selective catalytic reduction (SCR) waste catalyst. The process includes the following steps: a, preprocessing the SCR waste catalyst and leaching at the high temperature and under high pressure; b, adding hydrochloric acid into leaching liquid, adjusting pH, and removing impurities; c, adding hydrochloric acid into the leaching liquid, reacting, calcining and preparing rutile titanium dioxide; d, preparing ammonium paratungstate; e, preparing ammonium metavanadate; and f, recycling and treating waste water. Main products of ammonium paratungstate, ammonium metavanadate and rutile titanium dioxide obtained in the process are high in purity and recovery rate. By-products of silicon magnesium slags, salty mud, high-concentration sodium chloride liquid and barium sulfate dregs are high-purity harmless useful goods. The process is free of harmful secondary pollutant emission, environment-friendly and capable of circulating, has high economical and social benefit and is practicable.