• 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:
    1489015 Working up titanium dioxide hydrate suspensions BAYER ANTWERPEN NV 14 May 1975 [17 May 1974] 20310/75 Heading ClN In a process for working up an aqueous titanium dioxide hydrate suspension in one or more filtration and washing stages, the suspension is filtered under a pressure of 1-16 bars gauge, preferably 3-6 bars, and converted into a homogeneous, substantially crack-free filter cake with a layer thickness of 10-35 mm. The filter cake may be washed under a pressure of 1-16 bars, preferably 4-10 bars by passing the washing liquid through the filter cake at flow rates of 0À1-1À0 m./h. Ti(III) may be added to the washing water in concentrations of 0À8-4À0 g./l. A membrane filter which comprises horizontal filter compartments which enable filter cakes to be obtained in a layer of controlled thickness is preferably used. The solids content of the cake may be raised to above 45% by weight. The filter cake may be chemically treated before calcination, e.g. at 600-1, 200‹ C. to form TiO 2 in anatase or rutile form.
    公开号:SU841595A3
    申请号:SU752133715
    申请日:1975-05-15
    公开日:1981-06-23
    发明作者:Вейлер Рауль；Увентс Генри
    申请人:Байер Антверпен Н.Ф. (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to the production of titanium dioxide, in particular to methods for processing aqueous suspensions of titanium dioxide hydrate into pigment titanium dioxide used in the paint and varnish industry.
    It is known that titanium dioxide, in particular in pigment form, is obtained by the sulfate technology pu ~. by treating titanium-containing, for example, 10 ilmenite, ores with sulfuric acid, hydrolyzing the resulting titanium sulfate solution, forming a suspension of precipitated titanium hydroxide, followed by filtration of the latter, washing, bleaching, surface treatment and calcining the precipitate of titanium hydroxide separated by filtration moreover, the titanium dioxide hydrate obtained by hydrolysis is usually separated from the suspension using vacuum filters, which allow simultaneously washing the precipitate of hydrocaps isi £ 1].
    However, such washing allows to reduce the iron content in the sediment to 0.1 wt.%, Which is insufficient.
    There is also known a method of processing an aqueous suspension of titanium dioxide hydrate into a pigment, according to which the suspension after hydrolysis is filtered using a vacuum or rotating filter and the precipitate separated therein is washed to remove impurities, providing a reduction of iron impurity to 4-10 *% or less at interference with the washing liquid containing Ti + * ions. The precipitate of titanium hydroxide thus washed is calcined to form pigment titanium dioxide [2].
    However, this method does not provide a sufficiently high purification of the precipitated titanium hydroxide from undesirable iron impurities, which degrade the brightness of the target pigment.
    In addition, the specified limits of filtration and washing are quite long and provide a solid content in the filtered paste of not more than 35-40 wt.% Ti0 2 , the large moisture capacity of the precipitate requires large energy consumption for evaporation of excess moisture during calcination.
    The purpose of the invention is to reduce the iron impurity in the pigment energy consumption when it is set. The goal is that, according to the method and the reduction of calcination, it is achieved by processing an aqueous suspension of titanium dioxide hydrate into pigment, filtering is carried out at a pressure of 4 ^ 6 bar, and the precipitate separated by washing is washed at 4-10 bar followed by annealing. The present invention allows to reduce the content of iron impurities in the pigment by about 1.5-2.0 times, ie, to 1.8-2.5 · 10 “3%.
    In addition, due to the increase. the amount of solid in the filtered and washed precipitate of hydroxide up to 45-55 wt.% significantly reduces the energy consumption for its calcination (by 10-30%) and the process is intensified.
    In these pressure conditions, the filtration process of hydrated titanium dioxide precipitated after hydrolysis is also intensified and accelerated. The implementation technology of the proposed method is as follows. As a filter apparatus, mainly membrane-type filters are used, as well as filters
    Mura or rotating, having horizontal chambers and allowing to operate with filter deposits within 10-35 mm. h ;
    t Filtration is combined with one or more washing steps. The latter is carried out directly on the filter. In this case, the washing liquid is passed through a filter cake or filter at a speed of 0.1-1 m / h, preferably 0.3-0.7 m / h.
    It is envisaged in the washing water to add titanium (til) to a concentration of 0.8-4 g T | ^ + / l ”35
    Example 1 .: A suspension of hydrated titanium dioxide is filtered on a membrane filter at a pressure of 4 bar for 2 minutes, then the precipitate is pressed from it to a thickness of 15-25 mm at 16 bar for min, dry blasting is performed at a bar for 1 min and shutter speed 3.5 min. The anatase hydroxide product is filtered with a growth rate of the order of 120-130 kg / m ^ h ____ of the filter surface of 2.5 m 2 · (based on T10 2 ). The performance of the radio rutile hydroxide is lower in this case by 20%. Moreover, in the case of anatase, the solids content in the $ 0 precipitate is adjusted to 50 wt.%, And in the case of rutile to 48.5 wt.%.
    Example 2. Analogously to example 1, filtering and washing a suspension of titanium hydroxide on a 55 membrane filter and then pressing under the conditions and sequence shown in the table.
    with scopri 45 filter
    Time.
    Filtration at 4-4.5 bar Flushing at 6-8 bar and a fluid flow rate of 0.38 m / h
    2.5 .60.
    VNIIIPI Order 4878/85
    Continue e tab. Operation' Time,min Crimping at 16 bar 3 Dry blast at 4-4.5 bar 0.5 General pause of the device 3,5
    Filtration performance for anatase is 44.2 kg / m2, and for rutile 20% less. The maximum thickness of the sediment is 15-25 mm. The iron content in the precipitate is 2 · 10 * ^%, solid as in Example 1.
    PRI me R * 3. A hydrolyzed suspension of titanium hydroxide in rutile form is filtered on a membrane filter with a filter surface
    2.5 pressure of 6 bar with a filtration rate of 8 kg / m 2-h for rutile and 10-15 kg / m 2.h for anatase for 10 min. The precipitate is further washed with water at b bar at a flow rate
    6.56 m / h-10 min, press it at b bar for 4 min, re-washed with water with a content of 1.5 g T | 3 + / l at b bar and a flow rate of 0.25 m / h for 46 min, the sediment is pressed again at 16 bar for 3 min, dry blown at 4 bar for 1 min and the apparatus is kept for 3.5 min. The total processing time of the suspension in this way is
    77.5 minutes
    After dry blasting, the iron content in the filter cake is 2.5- , 10 ~ ^%, and the solid content is 50%. The maximum thickness of the filter cake is 1525 mm.
    Next, the precipitate is calcined in a kiln to obtain the finished pigment in the form of rutile or anatase.
    权利要求:
    Claims (1)
    [1]
    Claim
    A method of processing an aqueous suspension of titanium dioxide hydrate into a pigment by filtering it, washing the precipitate and calcining it, characterized in that, in order to reduce the impurity of iron in the target product and to reduce energy consumption for calcining, filtering the suspension and washing the precipitate, pressurize 4-6 and 4-10 bar, respectively.
    类似技术:
    公开号 | 公开日 | 专利标题
    EP0657385B1|1998-01-07|Titanium dioxide slurries
    SU841595A3|1981-06-23|Method of processing titanium dioxide hydrate suspension into pigment
    US5030439A|1991-07-09|Method for producing particulate titanium oxides
    DE1592406A1|1970-12-17|Process for the production of titanium dioxide pigments with a high degree of whiteness
    US4676959A|1987-06-30|Bayer process for producing aluminum hydroxide having improved whiteness
    US4786482A|1988-11-22|Bayer process for producing aluminum hydroxide having improved whiteness
    CN101077945A|2007-11-28|Method for producing ferric oxide black pigment from titanium pigment waste slag copperas
    RU2656047C1|2018-05-30|Method of obtaining iron oxide pigments
    US5094834A|1992-03-10|Process for the production of tio2 pigments
    AU742966B2|2002-01-17|Pure titanium dioxide hydrate and a process for the production thereof
    US3528773A|1970-09-15|Method of preparing titanium dioxide pigment
    US2148283A|1939-02-21|Preparation of white titanium dioxide pigments
    SU1393835A1|1988-05-07|Method of producing titanium dioxide pigment
    SU1085935A1|1984-04-15|Method for preparing titanium dioxide pigment of anathase modification
    SU643520A1|1979-01-25|Method of obtaining pigment titanium dioxide
    SU1044651A1|1983-09-30|Method for processing manganese ores and sludges
    CN1111510C|2003-06-18|Process for preparing activated zinc oxide
    SU1451097A1|1989-01-15|Method of producing titanium dioxide
    CN114014355A|2022-02-08|Method for purifying and deironing industrial metatitanic acid
    SU1677076A1|1991-09-15|Method of dechlorination of zinc solutions
    RU2102324C1|1998-01-20|Method for producing titanium dioxide
    US2403248A|1946-07-02|Iron hydrate and the manufacture and of use the same
    RU2312065C1|2007-12-10|Method of production of the chemically deposited chalk
    SU670596A1|1979-06-30|Method of producing pigment titanium dioxide
    SU975576A1|1982-11-23|Method for surface treatment of titanium dioxide pigment of the rutile modification
    同族专利:
    公开号 | 公开日
    CS197246B2|1980-04-30|
    IT1040591B|1979-12-20|
    NL7505671A|1975-11-19|
    ES437754A1|1977-05-16|
    AU8104075A|1976-11-18|
    US3981978A|1976-09-21|
    NO140181C|1979-07-18|
    CA1072885A|1980-03-04|
    DE2423983C3|1978-09-07|
    FI751432A|1975-11-18|
    NO140181B|1979-04-09|
    DE2423983A1|1975-12-04|
    BR7503060A|1976-04-13|
    GB1489015A|1977-10-19|
    NO751598L|1975-11-18|
    DE2423983B2|1977-12-15|
    FR2271174B1|1980-08-22|
    HU171549B|1978-02-28|
    JPS50160198A|1975-12-25|
    BE829189A|1975-11-17|
    FR2271174A1|1975-12-12|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2148283A|1936-05-11|1939-02-21|Nat Lead Co|Preparation of white titanium dioxide pigments|
    FR1422120A|1964-09-21|1965-12-24|British Titan Products|Improved process for preparing pigmentary titanium oxide|US5536529A|1989-05-11|1996-07-16|Borden, Inc.|Ultraviolet radiation-curable coatings for optical fibers and optical fibers coated therewith|
    US5352712A|1989-05-11|1994-10-04|Borden, Inc.|Ultraviolet radiation-curable coatings for optical fibers|
    US4978396A|1989-05-12|1990-12-18|Kerr-Mcgee Chemical Corporation|Process for preparing high solids slurries|
    DE3921262C1|1989-06-29|1990-07-05|Bayer Ag, 5090 Leverkusen, De|
    DE3938693C2|1989-11-22|1993-12-02|Bayer Ag|Process for the preparation of TiO 2 O 2 pigments|
    DE4238087C3|1992-11-11|1997-12-04|Bokela Ing Gmbh|Process for mechanical dehumidification of a filter cake and device for carrying out the process|
    US6409929B2|1992-11-11|2002-06-25|Bokela Ingenieurgesellschaft Fur Mechanische Verfahrenstechnik Mbh|Steam drying of rotary filter cakes without crack formation|
    US6048505A|1997-06-16|2000-04-11|Kemicraft Overseas Limited|Continuous non-polluting liquid phase titanium dioxide process and apparatus|
    DE19806471A1|1998-02-17|1999-08-19|Kerr Mcgee Pigments Gmbh & Co|Pure titanium dioxide hydrate and process for its production|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE2423983A|DE2423983C3|1974-05-17|1974-05-17|Process for the preparation of aqueous titanium dioxide hydrate suspensions by pressure filtration|
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