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44results about "Stannic chloride" patented technology

Gecl4 and/or sicl4 recovery process from optical fibers or glassy residues and process for producing sicl4 from sio2 rich materials

A method is provided for producing GeCl4 with or without SiCl4 from optical fibers, the method comprises the steps of: reacting comminuted optical fibers including germanium and optionally silicon oxides with a reagent including a solid carbonaceous reducing agent, chlorine and a boron compound to obtain a gaseous product including gaseous GeCl4, gaseous SiCl4, and gaseous BCl3 in accordance with the reactions: 2BCl3(g)+1.5GeO2=1.5GeCl4(g)+B2O3; 2BCl3(g)+1.5 SiO2=1.5 SiCl4(g)+B2O; B2O3+1.5C+3Cl2=2BCl3(g)+1.5CO2; and then condensing the gaseous GeCl4, BCl3 and optionally SiCl4 into liquid GeCl4, BCl3 and optionally SiCl4. The invention further provides a method for producing SiCl4 (and optionally GeCl4) from glass residues obtained from optical fiber manufacturing and wasted optical cables. The method includes the steps of: reacting comminuted glassy residues with a reagent including a solid carbonaceous reducing agent, a salt, a boron compound to obtain a gaseous product including SiCl4, BCl3, and optionally GeCl4; and then condensing the gaseous SiCl4, BCl3 (with or without GeCl4) into liquid SiCl4, BCl3 and GeCl4. There is also provided a method for producing SiCl4 from a SiO2 containing material.
Owner:INSTITUT NATIONAL DE LA RECHERCHE SCIENTIFIQUE

Method for producing tin chloride and elemental mercury by using mercury-containing waste catalyst

The invention relates to a method for producing tin chloride and elemental mercury by using a mercury-containing waste catalyst, which relates to the technical field of three-waste treatment and utilization of an organic industrial waste mercury catalyst. The tin chloride and elemental mercury can be obtained by the following three steps: the waste mercury catalyst is sent to a sealed-type distiller for distillation, mercuric chloride is directly sublimated to gas, then cooled to mercuric chloride liquid; then an above mercuric chloride solution and stannous chloride are subjected to a reaction, a mixing solution of tin chloride and the elemental mercury is generated; the mixing solution is subjected to enclosed pumping filtration to obtain a filter cake elemental mercury, then the filter cake elemental mercury is washed, dehydrated and packaged to obtain the elemental mercury product; and finally the tin chloride solution is sent to a normal pressure distiller for distillation, when tin chloride reaches a saturated solution, cooling crystals are discharged, and crushed and packaged to obtain the tin chloride crystals finished product. The method effectively prevents pollution of the waste mercury catalyst on environment, performs comprehensive utilization on the waste mercury catalyst, and provides high economic benefit for the enterprises at the same time.
Owner:常德湘大环保科技有限公司

Method for preparing active iron oxide powder materials by means of vacuum aluminothermic reduction

The invention relates to a method for preparing active iron oxide powder materials by means of vacuum aluminothermic reduction. Iron sesquioxide micro-powder is used as a raw material, aluminum micro-powder is used as a reducing agent, and the iron oxide powder materials can be manufactured by the aid of a vacuum aluminothermic reduction process. The method includes preparing steps of 1, uniformly mixing the iron sesquioxide micro-powder, namely, the raw material, and the aluminum micro-powder, namely, the reducing agent, with each other to obtain mixtures for standby application; 2, placing the mixtures obtained in the step 1 in the center of a clean porcelain boat; 3, placing the porcelain boat prepared in the step 2 in the middle of a high-temperature tube furnace, sealing the tube furnace, pumping the high-temperature tube furnace by the aid of a vacuum pump to enable the high-temperature tube furnace to be in an internal negative-pressure state and keeping the vacuum degree of the high-temperature tube furnace lower than or equal to 5pa; 4, heating the high-temperature tube furnace until the temperature of the high-temperature tube furnace reaches 900-1000 DEG C, keeping the raw material and the reducing agent reacting to each other for certain reaction time, then stopping heating the high-temperature tube furnace, cooling the high-temperature tube furnace until the temperature of the high-temperature tube furnace reaches the room temperature and taking products out of the high-temperature tube furnace. The method has the advantages that technologies are simple and controllable, prepared active iron oxide (FeO/Fe<3>O<4>, FeO, Fe/FeO) powder is high in purity and low in cost, and requirements of actual production can be met.
Owner:DONGGUAN PUREMATE ENVIRONMENTAL PROTECTION TECH CO LTD

Synthesis method of molybdenum trichloride

PendingCN114132963AImprove qualityEmission reductionStannic chlorideMolybdenum halidesTetrachlorideMolybdenum(III) chloride
The invention discloses a process for preparing molybdenum trichloride, which comprises the following steps of: (1) mixing excessive molybdenum pentachloride and stannous chloride powder, and heating the mixed material in a reactor to carry out replacement reaction to generate molybdenum trichloride and stannic chloride; (2) gasifying the generated stannic chloride, leaving the reactor, entering a cooling system for receiving and cooling to obtain stannic chloride liquid; (3) after the reaction is completed, switching a cooling system into a molybdenum pentachloride receiver, heating the reactor to a certain temperature, and gasifying redundant molybdenum pentachloride into the molybdenum pentachloride receiver; and (4) cooling the reactor, and discharging to obtain a molybdenum trichloride product. And (5) hermetically filtering the tin tetrachloride liquid to obtain a tin tetrachloride product and molybdenum pentachloride filter residues, wherein the molybdenum pentachloride filter residues and cooled and collected molybdenum pentachloride can be recycled as reaction raw materials. According to the method, the yield of molybdenum trichloride is increased, meanwhile, the production cost is reduced, the purity of the by-product tin tetrachloride exceeds 99%, the waste gas amount in the production process is greatly reduced, and the method belongs to a green and environment-friendly process.
Owner:湖南省华京粉体材料有限公司

Tin tetrachloride production device with wave tube reactor

The invention discloses a tin tetrachloride production device with a wave tube reactor. The tin tetrachloride production device comprises a tin smelting furnace, a pressurizing tank, a condensing tube, a chlorine gas storage tank, a cyclone separating tank and a product storage tank, wherein the tin smelting furnace is connected to the pressurizing tank; the interior of the tin smelting furnace is provided with the wave tube reactor; the wave tube reactor comprises a reaction pipeline with a tube body as a wave tube body, two inlet tubes and a product outlet tube; the bottom of the pressurizing tank is connected with a tin liquor feeding tube; the tail end of the tin liquor feeding tube is connected to any inlet tube of the wave tube reactor; the outlet of the chlorine gas storage tank is connected with a tee joint; one outlet of the tee joint is connected to the other inlet tube of the wave tube reactor through the chlorine gas inlet tube; another outlet of the tee joint is connected to the top of the cyclone separating tank; the product outlet tube of the wave tube reactor is connected to the cyclone separating tank through the condensing tube; the bottom of the cyclone separating tank is connected to the product storage tank. The tin tetrachloride production device not only can realize continuous production, but also can be high in reaction speed, high in yield and almost free of pollution on environment.
Owner:NANYANG NORMAL UNIV

Method for preparing anhydrous stannic chloride

The invention relates to the field of deep processing of tin, in particular to a process for preparing anhydrous stannic chloride. The process comprises the following steps: tin particles are melted; a fluid formed after melting of the tin particles is perpendicularly sprayed to the surface of a roller rotating at a high speed from top to bottom through a spray nozzle; the fluid is thrown to an atomization chamber on one side due to rotation of the roller, and tin drops are formed; chlorine is introduced to the atomization chamber from bottom to top to be subjected to a reaction with the tin drops; the mixture is sprayed to a collection chamber on one side of the atomization chamber; chlorine is collected from the upper side of the collection chamber; liquid stannic chloride is collected from the lower side of the collection chamber; the collected chlorine is conveyed to the atomization chamber again to be recycled; the collected liquid stannic chloride is gasified and condensed, and the anhydrous stannic chloride is obtained. The sprayed fluid is broken under centrifugal force of the rotating roller, chlorine collides with the tin drops at a high speed and is mixed sufficiently with the tin drops to be subjected to a reaction, the reactants can be sufficiently mixed and then sprayed to the collection chamber through a sprayer, and collection of a product and chlorine is greatly facilitated.
Owner:广东千千省化工有限公司

A kind of method for preparing anhydrous tin tetrachloride

The invention relates to the field of deep processing of tin, in particular to a process for preparing anhydrous stannic chloride. The process comprises the following steps: tin particles are melted; a fluid formed after melting of the tin particles is perpendicularly sprayed to the surface of a roller rotating at a high speed from top to bottom through a spray nozzle; the fluid is thrown to an atomization chamber on one side due to rotation of the roller, and tin drops are formed; chlorine is introduced to the atomization chamber from bottom to top to be subjected to a reaction with the tin drops; the mixture is sprayed to a collection chamber on one side of the atomization chamber; chlorine is collected from the upper side of the collection chamber; liquid stannic chloride is collected from the lower side of the collection chamber; the collected chlorine is conveyed to the atomization chamber again to be recycled; the collected liquid stannic chloride is gasified and condensed, and the anhydrous stannic chloride is obtained. The sprayed fluid is broken under centrifugal force of the rotating roller, chlorine collides with the tin drops at a high speed and is mixed sufficiently with the tin drops to be subjected to a reaction, the reactants can be sufficiently mixed and then sprayed to the collection chamber through a sprayer, and collection of a product and chlorine is greatly facilitated.
Owner:广东千千省化工有限公司
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