SU1472444A1 - Method of producing finely particulate silicon dioxide - Google Patents
Method of producing finely particulate silicon dioxide Download PDFInfo
- Publication number
- SU1472444A1 SU1472444A1 SU874198947A SU4198947A SU1472444A1 SU 1472444 A1 SU1472444 A1 SU 1472444A1 SU 874198947 A SU874198947 A SU 874198947A SU 4198947 A SU4198947 A SU 4198947A SU 1472444 A1 SU1472444 A1 SU 1472444A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- stage
- silicon dioxide
- temperature
- cooling
- sio
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/113—Silicon oxides; Hydrates thereof
- C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
- C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
- C01B33/181—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by a dry process
- C01B33/183—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by a dry process by oxidation or hydrolysis in the vapour phase of silicon compounds such as halides, trichlorosilane, monosilane
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Silicon Compounds (AREA)
Abstract
Изобретение касаетс получени пирогенной двуокиси кремни , примен емой в качестве наполнител в полимерных материалах, загустител жидкофазных композиций, при получении адсорбентов и носителей катализаторов, и позвол ет понизить энергоемкость процесса. Продукты реакции гидролиза галогенида кремни в воздушноводородном пламени после выхода из реактора с температурой 450°С и выше поступают на первую стадию разделени , где при температуре не менее 400°С улавливаетс основна часть SIO2, не требующа последующей очистки. Оставша с часть SIO2 вместе с газообразными продуктами реакции гидролиза поступает на стадию охлаждени и коагул ции частиц SIO2. Температура аэрозольной смеси после стадии охлаждени и коагул ции составл ет 120-175°С. Окончательное разделение аэрозольной смеси осуществл ют на второй стадии разделени в циклонах при температуре 100-150°С. Уловленна на второй стадии разделени двуокись кремни подвергаетс очистке от адсорбированных примесей хлора и хлористого водорода при повышенных температурах (400-700°С), а газообразные продукты поступают на стадию абсорбции хлористого водорода и хлора. 1 табл.The invention relates to the preparation of pyrogenic silicon dioxide, used as a filler in polymeric materials, a thickening agent for liquid phase compositions, in the preparation of adsorbents and catalyst carriers, and reduces the energy intensity of the process. The products of the hydrolysis reaction of silicon halide in an air-hydrogen flame after exiting the reactor with a temperature of 450 ° C and above enter the first separation stage, where, at a temperature of at least 400 ° C, the main part of SIO 2 is captured, which does not require further purification. The remaining part of SIO 2 together with the gaseous products of the hydrolysis reaction enters the stage of cooling and coagulation of SIO 2 particles. The temperature of the aerosol mixture after the cooling and coagulation step is 120-175 ° C. The final separation of the aerosol mixture is carried out in a second separation stage in cyclones at a temperature of 100-150 ° C. The silica caught in the second separation stage is purified from adsorbed chlorine and hydrogen chloride impurities at elevated temperatures (400-700 ° C), and gaseous products enter the hydrogen chloride and chlorine absorption stage. 1 tab.
Description
445°С. Далее смесь поступает в циклон на первую стадию разделени . Температура смеси в циклоне . В результате, на первой стадии раз- делени получают 29,9 кг/ч (80,1% от общего количества) высокодисперсной двуокиси кремни , соответствующей требовани м ГОСТ 14922-77 и не требующей дополнительных затрат на очистку от адсорбированных примесей НС1 и Cl(j.445 ° C. The mixture then enters the cyclone in the first separation stage. The temperature of the mixture in the cyclone. As a result, in the first stage of separation, 29.9 kg / h (80.1% of the total amount) of highly dispersed silicon dioxide, which meets the requirements of GOST 14922-77 and does not require additional costs for the removal of adsorbed impurities HC1 and Cl ( j.
Газообразные продукты реакции гидролиза и неуловленна в циклоне двуокись кремни проход т через ста- дню коагул ции и охлаждени смеси до 105°С. При этой температуре осуществл ют в циклоне вторую стадию раздапени . В результате получают 7,5 кг/ч 19,9% от общего количества высокодисперсной двуокиси кремни , которук подвергают дополнительной очистке от адсорбированных примесей хлористого водорода и хлора путем термообработки при 500°С.The gaseous products of the hydrolysis reaction and silicon dioxide not captured in the cyclone pass through the coagulation and cooling phase of the mixture to 105 ° C. At this temperature, the second stage of decomposition is carried out in a cyclone. As a result, 7.5 kg / h of 19.9% of the total amount of highly dispersed silicon dioxide is obtained, which is further subjected to additional purification from adsorbed impurities of hydrogen chloride and chlorine by heat treatment at 500 ° C.
Газообразные продукты гидролиза (азот, кислород, хлористый водород, хлор, пары воды) поступают на -стадиюGaseous products of hydrolysis (nitrogen, oxygen, hydrogen chloride, chlorine, water vapor) are fed to the - stage
адсорбции хлористого водорода и хлора ,adsorption of hydrogen chloride and chlorine,
Удельные энергозатраты составл ют 3,68 кВт-ч/кг Si02, в том числе энергозатраты на термообработку - 0,25 кВт-ч/кг Bi02.The specific energy consumption is 3.68 kWh / kg Si02, including the energy consumption for heat treatment — 0.25 kWh / kg Bi02.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU874198947A SU1472444A1 (en) | 1987-01-05 | 1987-01-05 | Method of producing finely particulate silicon dioxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU874198947A SU1472444A1 (en) | 1987-01-05 | 1987-01-05 | Method of producing finely particulate silicon dioxide |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1472444A1 true SU1472444A1 (en) | 1989-04-15 |
Family
ID=21287282
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU874198947A SU1472444A1 (en) | 1987-01-05 | 1987-01-05 | Method of producing finely particulate silicon dioxide |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU1472444A1 (en) |
-
1987
- 1987-01-05 SU SU874198947A patent/SU1472444A1/en active
Non-Patent Citations (1)
Title |
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Авторское свидетельство СССР № 1247340, кл. С 01 В 33/18, 1984. * |
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