专利摘要:
The invention relates to a method for producing active alumina. The purpose of the invention is to simplify and reduce the cost of technology. Metal aluminum depassiviruyut. in a nitric acid solution containing 0.5-1.0 g / l of mercury. Then anodic dissolution is carried out in a solution of nitric acid using an aluminum-graphite galvanic pair. Removal of the precipitate of aluminum hydroxide and the introduction of a solution of nitric acid lead-periodically after 1-3 days. The resulting aluminum hydroxide is dried and calcined. 1 3.p. f-ly, 1 tab. SU) with ate JV GO see
公开号:SU1355120A3
申请号:SU833658449
申请日:1983-11-04
公开日:1987-11-23
发明作者:Манди Тамаш;Немет Ласло;Керти Йожеф;Грофчик Элемер;Керекеш Андраш
申请人:Мадьяр Сенхидрогенипари Кутато-Фейлесте Интезет (Инопредприятие);Кепорц Электроникаи Алькатрес Еш Мюсаки Керамиадьярто Валлалат (Инопредприятие);
IPC主号:
专利说明:

The invention relates to a method for producing active alumina. The aim of the invention is to simplify and reduce the cost of technology.
Example 1. In a plastic cylindrical vessel with a capacity of 200 liters, 12 rods of refined aluminum weighing 5 kg and graphite each are placed. The aluminum rods are pretreated for 15 minutes with an activating aqueous monomoleric nitric acid solution containing 0, & g / l of mercury ions to the immersion depth. Approximately 80 l of a two-molar solution of nitric acid is poured into the container, and all aluminum and graphite rods are connected by means of a pre-conductor to a common anodic and cathodic busbar. In the current circuit obtained by such a short-circuited cell, a high-power rheostat and an ammeter are included.
Using a rheostat at the beginning of a highly heated cell, the current is reduced to less than 100 A to prevent boiling of the solution. As a result of the dissolution of aluminum and an increase in the content of nitrate ions in the cell, the pH stabilizes in the range of 3.9-4.1 and the process begins. gel formation of aluminum hydroxide. From the moment of stabilization of the pH, the magnitude of the current in the cell is established within 15A with a fully removed rheostat, and the content of the cell is cooled to room temperature.
After three days, the gel collected in the lower part is removed, and the well is filled with a new solution of nitric acid. The process is carried out until the aluminum rods are almost completely dissolved. The gel withdrawn from the cell is centrifuged to remove the mother liquor, then extruded to obtain bars with a diameter of 1.5 mm, dried and heat-treated.
500-700 C to obtain high-purity alumina y-modification.
Example 2. The process is carried out under the conditions specified in Example I, with the difference that 6 cells are simultaneously operated, the aluminum and graphite rods of which are connected to the common anodic and cathode walls in parallel. Every 8 hours, the solution is renewed in two cells in succession.
As a result, the hydroxide gel formed is removed from each cell once a day.
The properties of the obtained aluminum oxide U-modification are given in the table.
The invention allows technology to be reduced by reducing power consumption and reducing costs by simplifying the processing circuitry.
0
five
0
five
权利要求:
Claims (2)
[1]
1. A method of producing active alumina, including anodic dissolution of metallic aluminum in a solution containing 1 mol / l of nitrate ions, to produce aluminum hydroxide, then drying it and calcining to obtain aluminum oxide, which differs (5 in order to simplify and cheaper technology, before dissolving, metallic aluminum is depassivated by immersion in a nitric acid solution containing 0.5-1.0 g / l of mercury, anodic dissolution is carried out in a solution of nitric acid using an aluminum-graphite galvanic couple
[2]
2. The method according to claim 1, 2 and 5, so that the anodic dissolution is carried out with the combination of several electroplating pairs in parallel with the periodic removal of the precipitate of aluminum hydroxide and the introduction of a solution of nitric acid after 1-3 days.
Editor R. Volkova
Compiled by N.Novikov Tehred M.Hodanich
Order 5719/57 Circulation 456 Subscription
VNIIPI USSR State Committee
for inventions and discoveries 113035, Moscow, Zh-35, Raushsk Nab., 4/5
Production and printing company, Uzhgorod, Projecto st., 4
Proofreader M.Sharoshi
类似技术:
公开号 | 公开日 | 专利标题
SU1355120A3|1987-11-23|Method of producing active aluminium oxide
DK166735B1|1993-07-05|PROCEDURE FOR ELECTROLYTIC RECOVERY OF LEAD FROM LEAD WASTE
SU738518A3|1980-05-30|Leads of powerful aluminium electrolyzers
GB1151943A|1969-05-14|Improvements in or relating to the Etching of Metallic Copper
KR100425662B1|2004-05-20|Basic Cobaltous Carbonates, Process for Preparing the Same and Their Use
CA1106798A|1981-08-11|Process for producing tin | sulfate
CH610935A5|1979-05-15|Electrochemical reactor intended to be incorporated into a plant for the production of titanium dioxide from ilmenite by the sulphate process
JPS63195101A|1988-08-12|Production of metallic oxide
SU507561A1|1976-03-25|Method for producing cotarnine and opic acid
SU1244212A1|1986-07-15|Method of anodizing aluminium
KR890012019A|1989-08-23|Synthesis of metal salts of weak acids, especially indium formate
SU1313891A1|1987-05-30|Method of producing magnesium oxide
SU1440943A1|1988-11-30|Method of purifying zinc sulfate solutions from copper and cadmium
SU607782A1|1978-05-25|Method of purifying green copperas
SU905199A1|1982-02-15|Process for preparing trivalent titanium sulphide solution
SU1224269A1|1986-04-15|Method of removing organic dyes from waste water
SU517593A1|1976-06-15|Method for producing cotarnine and opic acid
SU1608250A1|1990-11-23|Method of producing nitronium salts
SU396420A1|1973-08-29|METHOD OF ELECTROLYTIC DEPOSITION OF TIN FROM ACIDIC SOLUTIONS
JPS5620186A|1981-02-25|Treatment of dross contained copper and lead
CN112174971A|2021-01-05|Purification method of spiro quaternary ammonium tetrafluoroborate
SU1121322A1|1984-10-30|Method for preparing solution for electrolytic refining of nickel
SU136149A1|1960-11-30|Bare copper anodes
SU876792A1|1981-10-30|Method of regenerating copper electrolyte
JPH07188965A|1995-07-25|Method for recovering copper from copper sulfide
同族专利:
公开号 | 公开日
EP0108968A1|1984-05-23|
DD230885A1|1985-12-11|
HU189188B|1986-06-30|
AT32106T|1988-02-15|
DE3375407D1|1988-02-25|
EP0108968B1|1988-01-20|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
RU2664135C1|2017-07-17|2018-08-15|Федеральное государственное бюджетное учреждение науки Институт химии высокочистых веществ им. Г.Г. Девятых Российской академии наук |Method of electrochemical obtaining of aluminum oxide powders|US3974055A|1974-12-23|1976-08-10|The Dow Chemical Company|Aluminum alloy anode composition|US20050124745A1|2002-04-19|2005-06-09|Saint-Gobain Ceramics & Plastics, Inc.|Flame retardant composites|
US20060104895A1|2004-11-18|2006-05-18|Saint-Gobain Ceramics & Plastics, Inc.|Transitional alumina particulate materials having controlled morphology and processing for forming same|
US7479324B2|2005-11-08|2009-01-20|Saint-Gobain Ceramics & Plastics, Inc.|Pigments comprising alumina hydrate and a dye, and polymer composites formed thereof|
EP2231523A2|2007-12-19|2010-09-29|Saint-Gobain Ceramics & Plastics, Inc.|Aggregates of alumina hydrates|
US8460768B2|2008-12-17|2013-06-11|Saint-Gobain Ceramics & Plastics, Inc.|Applications of shaped nano alumina hydrate in inkjet paper|
RU2466937C2|2010-12-21|2012-11-20|Андрей Павлович Лысенко|Method of obtaining aluminium oxide applicable for manufacturing artificial corundum crystals|
RU2742575C1|2020-10-14|2021-02-08|Общество с ограниченной ответственностью "Империус Групп"|Method for producing alpha-aluminium oxide for subsequent growth of single-crystal sapphire|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
HU823602A|HU189188B|1982-11-09|1982-11-09|Process for producing active aluminium-oxid|
[返回顶部]