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262 results about "Titanium trichloride" patented technology

Trivalent titanium. In titanium: Compounds …the more important is the trichloride TiCl3, a crystalline form of which is particularly useful as a catalyst in the stereospecific polymerization of propylene to make the commercially valuable polymer polypropylene.

Electrothermal film and manufacturing method thereof

The invention relates to an electrothermal film and a manufacturing method thereof, belonging to the technical field of semiconductor heating. The electrothermal film is mainly prepared by adopting stannic chloride, titanium tetrachloride, stannic chloride, titanium trichloride, ferric chloride, antimony trichloride, calcium chloride, potassium chloride, cadmium chloride, stannic dioxide, stannictetroxide, hydrofluoric acid, boric acid, ethanol, isopropyl alcohol and inorganic water. By adopting the above formula, the mixture is mixed, stirred and heated to prepare into electrothermal film treating fluid, a semi-finished product of the electrothermal film is obtained by spraying the electrothermal film treating fluid at negative pressure on the electrothermal film carrier, and then silveroxide slurry is coated on the semi-finished product of the electrothermal film for baking to form a finished product of the electrothermal film. The electrothermal film has reasonable proportion andsimple manufacturing process, can be manufactured into various electrothermal film heating devices, has a working temperature capable of being up to 500 DEG C, and has wider application range. The electrothermal film of the invention also has the function of far infrared radiation, can play a role of physical therapy and health care to human body, and can help improve the quality and output of agricultural products.
Owner:GUANGDONG HALLSMART INTELLIGENCE TECH CORP LTD

Methods for forming amorphous ultra-high molecular weight polyalphaolefin drag reducing agents

A composition including polyalphaolefins that function as drag reducing agents and a process for the preparation of polyalphaolefins that function as drag reducing agents are disclosed. The process includes contacting alpha olefin monomers with a catalyst system, which includes a catalyst and an activator (co-catalyst) in a reactant mixture. The catalyst is a transition metal catalyst, preferably titanium trichloride, and the co-catalyst may include an alkylaluminoxane, alone or in combination, with a dialkylaluminum halide or a halohydrocarbon. The polymerization of the alpha olefin monomers produces a non-crystalline, ultra-high molecular weight polyalphaolefin having an inherent viscosity of at least 10 dL/g. The addition of the alkylaluminoxane during the polymerization process provides for a non-crystalline, ultra-high molecular weight polyalphaolefin and a more uniform molecular weight distribution of the resulting polyalphaolefin, thereby creating a drag reducing agent superior to known drag reducing agents. A process for forming a drag reducing agent comprising a non-crystalline, ultra-high molecular weight polyalphaolefin having an inherent viscosity of about at least 10 dL/g and a process for reducing drag in a conduit are also disclosed.
Owner:MPOWER SPECIALTY CHEM

Method for removing iron and whitening for iron-containing attapulgite clay

The invention relates to a method for removing iron and whitening for iron-containing attapulgite clay, comprising the following steps of: (1) selecting ore the content of attapulgite of which is more than 40%, crashing the attapulgite clay, and screening the attapulgite clay by a 100-mesh sieve, roasting and activating the attapulgite clay for 1 hour at the temperature of 300 to 700 DEG C; (2) acidulating the attapulgite clay after roasting treatment by 3 to 8% sulfuric acid , wherein the mass ratio of the sulfuric acid solution to the attapulgite clay is 8:1; placing the attapulgite clay in the sulfuric acid, stirring and soaking for 4 hours at the temperature of 60 DEG C, then washing for many times by utilizing distilled water, controlling the pH value to be 6.0 to 7.0, drying at the temperature of 105 DEG C, and then grinding, screening by a 80 to 120 mesh sieve; and (3) preparing the attapulgite clay after acidification to 10 to 30% ore slurry, placing the ore slurry into a reaction vessel, adding oxalic acid with the concentration of 0.5 to 1.5 mol / L and 3 to 5% titanium trichloride, heating reaction vessel for 8 to 150 minutes, acidulating for 40 to 50 minutes, and centrifuging, washing and filtering after reaction, and drying at the temperature of 105 DEG C to obtain the white attapulgite clay.
Owner:LANZHOU UNIVERSITY OF TECHNOLOGY

Manufacturing method of electrothermal film

The invention discloses a manufacturing method of an electrothermal film. The manufacturing method comprises the following steps of A, preparing an electrothermal film treatment solution which comprises tin tetrachloride, titanium trichloride, antimony trichloride, calcium chloride, chromic oxide, manganese dioxide, nickel sesquioxide, isopropanol, alcohol and water, B, masking a substrate, C, heating the substrate to be 400-700 DEG C and then spraying the electrothermal film treatment solution on the substrate by a spray gun to form a semifinished electrothermal film, D, annealing the semifinished electrothermal film, and E, coating silver oxide paste on the surfaces of the two ends of the annealed semifinished electrothermal film, loading the semifinished electrothermal film into an electrode oven, baking and fusing the semifinished electrothermal film to form a whole, and obtaining the finished electrothermal film. The manufacturing method has the advantages that the stability of the electrothermal film is improved by adding antimony; the temperature resistance of the electrothermal film is improved by adding titanium; the infrared emitting ability of the electrothermal film is improved by adding nickel and manganese; and an adhesive force between the electrothermal film treatment solution and the substrate is increased by adding isopropanol.
Owner:成都世纪经尧科技有限公司

Aluminum product coated with nitrogen-doped graphene/nitrogen-doped TiO2 photo-catalytic material

The invention provides an aluminum product coated with a nitrogen-doped graphene/nitrogen-doped TiO2 photo-catalytic material. The aluminum product is prepared according to the following steps: preparing graphene oxide by using a method disclosed from the page 4806 to the page 4814 of volume 2010-4 of the journal of Nanometer of the American Chemical Society; adding deionized water, and performing ultrasonic dispersion to obtain graphene oxide dispersion liquid; respectively adding a hexamethylene tetramine solution and a titanium trichloride solution, uniformly mixing, performing hydrothermal reaction, centrifugally washing a precipitate, and drying to obtain the nitrogen-doped graphene/nitrogen-doped TiO2 composite photo-catalytic material; washing and drying an aluminum profile needing to be coated; adding the composite photo-catalytic material into acetonitrile or methyl methacrylate, and performing ultrasonic dispersion; and uniformly spraying the dispersion liquid onto the surface of the aluminum profile, and drying to obtain the aluminum product coated with the nitrogen-doped graphene/nitrogen-doped TiO2 composite photo-catalytic material. According to the aluminum product, photo-catalysis can be generated under the irradiation of indoor light, indoor air is purified, and indoor pollutants are reduced.
Owner:SHANGHAI RONGFU NEW MATERIAL

Methods for forming amorphous ultra-high molecular weight polyalphaolefin drag reducing agents using a halohydrocarbon

A composition including polyalphaolefins that function as drag reducing agents and a process for the preparation of polyalphaolefins that function as drag reducing agents are disclosed. The process includes contacting alpha olefin monomers with a catalyst system, which includes a catalyst and an activator (co-catalyst) in a reactant mixture. The catalyst is a transition metal catalyst, preferably titanium trichloride, and the co-catalyst may include an alkylaluminoxane, alone or in combination, with a dialkylaluminum halide or a halohydrocarbon. The polymerization of the alpha olefin monomers produces a non-crystalline, ultra-high molecular weight polyalphaolefin having an inherent viscosity of at least 10 dL / g. The addition of the alkylaluminoxane during the polymerization process provides for a non-crystalline, ultra-high molecular weight polyalphaolefin and a more uniform molecular weight distribution of the resulting polyalphaolefin, thereby creating a drag reducing agent superior to known drag reducing agents. A process for forming a drag reducing agent comprising a non-crystalline, ultra-high molecular weight polyalphaolefin having an inherent viscosity of about at least 10 dL / g and a process for reducing drag in a conduit are also disclosed.
Owner:MPOWER SPECIALTY CHEM

Continuous and semi-continuous process of manufacturing titanium hydride using titanium chlorides of different valency

InactiveUS20110171116A1Reduce manufacturing costCost-effective and highly-productive manufactureTransition element hydridesTitanium chlorideOxygen
The invention relates to the manufacture of titanium hydride powder using continuous or semi-continuous process, and using titanium slag or synthetic rutile as raw materials, while hydrogen, titanium tetrachloride, titanium trichloride, titanium dichloride, and hydrogen chloride are participate as intermediate reaction products. The continuous comprises: (a) reduction of TiCl4 to low titanium chlorides followed by cooling a mixture, (b) separating of residual TiCl4 from solid low chlorides by heating the mixture in argon or vacuum up to 150° C. followed by removing the titanium tetrachloride from the mixture, (c) dissociation of TiCl3 to TiCl2 at 450° C. in vacuum followed by removal of gaseous titanium tetrachloride from the reaction zone, condensation to the liquid, and returning back into the reaction retort, (d) dissociation of TiCl2 in vacuum at 750-850° C. to manufacture fine powder of metallic titanium and titanium tetrachloride, whereby hydrogen heated up to 1000° C. is used to accelerate this reaction, and (e) saturation of the fine titanium powder by hydrogen at 400-640° C. to manufacture final product of titanium hydride powder which is free of oxygen or nitrogen. The semi-continuous process includes the Kroll's process as the very first step.
Owner:ADMA PRODS

High yield rapid synthesis method of titanium-silicon molecular sieve TS-1

The invention provides a high yield rapid synthesis method of a titanium-silicon molecular sieve TS-1. The synthesis method comprises the following steps: mixing raw materials namely a silicon source, a titanium source, tetrapropyl ammonium hydroxide and water according to a ratio of SiO2:TiO2:TPAOH:H2O of 1:(0.0501-0.099):(0.0501-0.1499):(0.101-4.999), wherein the silicon source is at least one of n-methyl silicate, n-ethyl silicate, silica sol, and white carbon black; the titanium source is at least one of tetraethyl titanate, tetrabutyl titanate, isopropyl titanate, titanium trichloride, and titanium tetrachloride; carrying out hydrolysis for 0-5 hours at a temperature of 30 to 60 DEG C, performing alcohol removal for 0 to 1 hour at a temperature of 90 DEG C, filling the hydrolysis product into a crystallization kettle, carrying out crystallization for 2 to 10 hours at a temperature of 210 to 250 DEG C; drying, and burning to obtain the titanium-silicon molecular sieve TS-1. The titanium-silicon molecular sieve TS-1 synthesized by the provided method has the advantages of high content of titanium in skeleton, little using amount of template, no generation of wastewater, and high crystallization speed. The particle size of obtained nano level titanium-silicon molecular sieve is about 100 nm. The titanium-silicon molecular sieve has an excellent catalytic performance on alkene epoxidation and aromatic hydrocarbon hydroxylation.
Owner:DALIAN UNIV OF TECH

Method for rapidly determining content of total iron in vanadium titano-magnetite

The invention provides a method for rapidly determining the content of total iron in vanadium titano-magnetite. The method comprises the following steps: (1) weighing a to-be-determined vanadium titano-magnetite sample with the weight of M; (2) adding sufficient mineral dissolving solution to dissolve the to-be-determined vanadium titano-magnetite sample in a heating manner; (3) adding dilute hydrochloride acid into a reaction vessel; (4) dropwise adding stannous chloride solution to the reaction vessel until the mixed solution turns pale yellow, reheating the mixed solution to be boiled slightly, and cooling the mixed solution to the room temperature; (5) adding sodium tungstate solution into the reaction vessel, dropwise adding titanium trichloride solution until the mixed solution turns blue, and dropwise adding titanium trichloride solution to be slightly excessive in volume; (6) dropwise adding potassium dichromate solution into the reaction vessel until the mixed solution is colorless, and dropwise adding sodium diphenylaminesulfonate indicator; (7) titrating the mixed solution in the reaction vessel to be purple by adopting potassium dichromate standard titration solution; (8) sampling the solution after being titrated to be purple, and determining the weight percentage of vanadium in the sample; and (9) calculating. The method is easy to operate, high in determination speed, capable of enabling the detection result to be equivalent to that of a national standard method and capable of better meeting the in-situ rapid analysis requirement.
Owner:武汉钢铁有限公司
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