• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1. Process for the preparation of lithium silicate according to which lithium carbonate and silica are intimately mixed and this mixture is then subjected to a heat treatment, characterized in the mixture is subjected to a precalcination heat treatment at a temperature of between 410 and 4408C so as to form in the mixture at least 25 % by weight of a hexagonal phase consisting of lithium, silicon and oxygen, the crystal parameters of which are : a = 3.06 8A and c = 4.97 8A.
    公开号:SU1533623A3
    申请号:SU853957950
    申请日:1985-09-20
    公开日:1989-12-30
    发明作者:Жан Пьер Флипо Альфред；Хенрикус Филомена Диелс Паулус；Жозеф Алексис Лекок Раймон
    申请人:Сантр Дъэтюд Де Лъ Энержи Нюклеэр "С.Э.Н." (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to methods for producing lithium silicate, which can be used as a lining material for smelting reactors for producing tritium.
    The purpose of the invention is to increase the specific surface area while ensuring the possibility of obtaining by sintering high-density granules with a density above 85% of theoretical density.
    Example 1. 190 g of lithium carbonate powder, 160 g of Aerosil powder (Degussa AG, Germany) with a specific surface area of 300 m / g were mixed with distilled water to obtain a paste-like mass. This paste was deposited for 60 minutes under water in an abrasive device, in which the balls and levers are made of alumina. This slurry is then continuously stirred to prevent delamination and spray dried.
    The resulting fine powder has a specific surface area.
    BY .
    I
    The powder is heat treated.
    in moist air saturated at room temperature at the beginning at 430 ° C for 30 hours to form a 25% hexagonal phase, and then calcined at 600 ° C for 16 hours and finally granulated at a pressure of 2.5 tons / cm in the matrix 6 mm diameter (hexagonal
    cl
    se
    I
    with

    sn
    BUT
    and
    15
    ase has parameters a 3.06 - 4.97 a).
    After sintering at 950 ° C in air for 9 hours, the granules have a density of 91.4% of the theoretical value.
    The same mixture precipitated for 2 hours instead of 1 hour, and after similar processing, the sintered granules had a density of 95% of the theoretical value, while the raw granules had a density of 48% of the theoretical value, they had a density of 98% of the theoretical value the density of raw granules is 50% of the theoretical value.
    Example 2. 272 g of lithium carbonate powder was mixed with 228 g of silica (Aerosil from Degus-20 AG, Germany) and water, precipitated for 60 minutes in an abrasive device and dried by spraying. The dried powder was precompressed into granules with a diameter of 25–12 mm under a pressure of 1.2 t / cmg. The granules were obtained on a grid with a cell of 1 mm, the manufactured granules were sequentially processed at 410 ° C for 6 hours, at 420 ° C for 16 hours and at 430 ° C for 8 hours in an atmosphere of humid air with a relative humidity of 30% before the formation of a 25% hexagonal phase with the parameters a 3,06 A, with 4,97 A, then granulation is carried out under a pressure of 2.5 t / cmg. The density of the granules reached 87.6% of the theoretical value when processed at 950 ° C for 3 hours and 81.1% of the theoretical value when processed at 950 ° C for 1 hour.
    Example 3. Heat-treated granules obtained in example 2, were subjected to calcination for 12 hours, and before this granulation was carried out under a pressure of 2.5 t / cmg. The density of the granules reached 93% of the theoretical value when processed at 925PC for 3 hours and 90% when processed at 50,950 ° C for 1 hour.
    Example 4. A mixture is prepared as in example 2, and the resulting powder is thermoablative at 440 ° C in moist air (water saturated 55
    at t 25eC), after 14 h, 25% of the hexagonal phase is formed with parameters a ≈ 3.06 A and with 4.97 A, then
    thirty
    35
    40
    45
    five
    Q
    0 5
    0
    five

    0
    lead calcination at 450 ° C for 10 h.
    The product is subjected to granulation and sintering for 3 hours at 925 C. The density of the granules reaches 91% of the theoretical value.
    Example 5. Powdered. lithium carbonate is mixed with silica and water, crushed for 30 min in a millstone and spray dried. The dried powder is compacted with cold isostatic compression under a pressure of 200 bar.
    The granules are then calcined in humid air with a relative humidity of 40% by slowly raising the temperature from 410 to 480 ° C for 70 hours, then the product is calcined for 3 hours at 700 ° C and granulated under a pressure of 1.2 tons / cm 2 to obtain granules with a diameter of 17 mm. Although “after heat treatment, the product was re-calcined at 700 ° C, sintering was satisfactory, and the density after calcination for 5 hours at 925 ° C was 95% of the theoretical value.
    Example 6. A lithium carbonate powder ground in a ball mill is mixed with silicon dioxide and water and dried by dissolving. The composition of the powder corresponds to the stoichiometric composition of lithium metasilicate. Saturated5
    metasilicate
    The powder is calcined in air, with water at 20 ° C, by slowly heating for 60 hours from 410 to 480 ° C. Then the product is re-calcined.
    0
    lott 1 t / cmg
    five
    for 5 hours at 600 ° C, packed and granulated under pressure
    After sintering at 950 ° С for 10 h, the density reaches 93% of the theoretical value.
    In all examples, a sintered lithium silicate was obtained having a density of at least 85% of the theoretical density. The known method does not allow high-density sintering products to be obtained, and does not give good-quality lithium silicate sintering products. The density of the prototype can be no higher than 78% of theoretical.
    A specific surface area of 15-60 is a mandatory characteristic of the intermediate product, which is only a pre-calcined or a mixture of pre-calcined and calcined products prior to the sinter product. This characteristic is important, since it is obvious that the higher the specific surface area of the intermediate powder, the higher the density of the final sintering product will be obtained.
    The specific surface of the intermediate powder products obtained in accordance with the invention, and the specific surface of the products obtained in accordance with the prototype, the result of the same processes, but without prior calcination.
    The specific surfaces according to the invention vary from 15 to 56 m2 / g but with calcination at 600 ° C for 24 hours, the specific surface will be equal to only 3.5 m / g,
    For example, if, according to known methods, spray-dried particles with a specific surface of 50 are used as the starting material, then after calcination only for 20 hours at L75 C, the specific surface of the barrel is 7 (increased to 9 if calcination is accompanied by a 3-minute grinding the mill).
    After preliminary calcination at 410-440 and calcination (20 hours at 675 ° C) in accordance with the invention, the specific surface area is 34 m / g.
    Thus, the density of the products prepared in accordance with the proposed process is significantly higher than those prepared by previously known processes, although the processes differ only in that in the context of the invention, a preliminary temperature treatment takes place at 410-440 ° C is absent in the known methods in which a hexagonal phase is not formed.
    权利要求:
    Claims (4)
    [1]
    1. A method of producing lithium silicate, which includes the heat treatment of a homogeneous mixture of lithium carbonate and silicon dioxide, followed by sintering the heat-treated mixture, characterized in that, in order to ensure the possibility of sintering high-density granules with a density above 85% of the theoretical
    Q density, heat treatment is carried out at 410-440 0 in an atmosphere of humid air from a relative humidity of 30% to saturated at room temperature humidity to form
    5 in a mixture of 25 wt.% Hexagonal phase with the parameters of crystals а ш 3.06 A and с 4.97 X ..
    [2]
    2. The method according to p. 1, is excellent - 1 and y with the fact that the heat treatment product before sintering is subjected to preliminary calcination
    at 450-600 ° C.
    [3]
    3. A method according to claim 1, characterized in that the heat treatment at 410-440 ° C is carried out for 145-30 hours.
    [4]
    4. The method according to claim 1, wherein the process is conducted by gradually increasing the temperature from 410 Ido B for 60-70 hours.
    0
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    同族专利:
    公开号 | 公开日
    EP0175423B1|1988-03-30|
    CA1241523A|1988-09-06|
    DE3562008D1|1988-05-05|
    JPS6177621A|1986-04-21|
    EP0175423A1|1986-03-26|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2083545A|1935-04-10|1937-06-15|Pennsylvania Salt Mfg Co|Process of making alkali sub-silicates|
    NL7406064A|1974-05-06|1975-11-10|Zinkwit Nederland B V|PROCESS FOR THE PREPARATION OF ANHYDROUS ALKALINE TASILICATES.|DE10255124A1|2002-11-26|2004-06-03|Degussa Ag|Fumed oxide powder, process for its preparation and its use in a separator for an electrochemical cell|
    CN101913616B|2010-08-13|2012-08-22|北京科技大学|Preparation method of lithium silicate material with high purity|
    CN103159222B|2011-12-09|2014-10-01|核工业西南物理研究院|Method of densification of lithium orthosilicate pellets used in tritium breeding|
    WO2013167723A1|2012-05-11|2013-11-14|Ivoclar Vivadent Ag|Pre-sintered blank for dental purposes|
    KR102018937B1|2012-05-11|2019-09-05|이보클라 비바덴트 아게|Pre-sintered blank for dental purposes|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    BE2/60505A|BE900642A|1984-09-20|1984-09-21|High specific surface lithium silicate prepn. - useful for blanket pellets in fusion reactors|
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