GB602453A - Synthetic forsterite materials - Google Patents
Synthetic forsterite materialsInfo
- Publication number
- GB602453A GB602453A GB16958/44A GB1695844A GB602453A GB 602453 A GB602453 A GB 602453A GB 16958/44 A GB16958/44 A GB 16958/44A GB 1695844 A GB1695844 A GB 1695844A GB 602453 A GB602453 A GB 602453A
- Authority
- GB
- United Kingdom
- Prior art keywords
- magnesia
- silica
- brine
- lime
- ingredients
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/16—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Treating Waste Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Synthetic magnesium orthosilicate for use in the manufacture of refractory materials is prepared by mixing together in the correct proportions magnesia and silica of sufficient fineness to unite without fusion, and heating the mixture to reaction temperature. The silica in particular and, preferably, the magnesia also, should comprise a considerable amount of particles approaching colloidal fineness. The silica which is preferably amorphous, may be that obtained as a waste product from the production of ferro-silicon, or the natural, finely divided materials such as chalcedony, geyserite or diatomaceous earth, or rice hull ashes may be used; alternatively, it may be obtained by reducing relatively-pure siliceous material such as quartz by heating with carbon, allowing the silicon to reoxidize, and collecting the product. The magnesia may be the dust obtained by electrostatic precipitation or otherwise from the flue gases of furnaces for calcining magnesite, precipitated magnesia, particularly that obtained by the treatment of seawater or brine with lime or calcined dolomite, or powdered calcined magnesite or brucite. In order to convert any lime and iron present in the ingredients into monticellite and magnesioferrite respectively, a slight excess of magnesia is employed, the proportions being 60 MgO to 40 SiO2. The ingredients are mixed together with a small amount of water, and cold-setting bonds, such as waste sulphite liquor, tar, sulphite pitch, molasses, or magnesium chloride or sulphate, may be incorporated. If magnesia precipitated from brine is employed, the mixture of the ingredients may be prepared by adding the finely-divided silica to the brine either before or after treatment with the lime. After mixing, the product may be shaped if desired, and the mixture is finally burnt at approximately 1450 C., or clinkers may be produced which are subsequently ground and bonded by the same or a different material. Specifications 579,098 and 602,454, [both in Group V], and U.S.A. Specifications 852,908 and 1,659,476 are referred to.ALSO:Synthetic magnesium orthosilicate for use in the manufacture of refractory materials is prepared by mixing together in the correct proportions magnesia and silica of sufficient fineness to unite without fusion, and heating the mixture to reaction temperature. The silica in particular and, preferably, the magnesia also, should comprise a considerable amount of particles approaching colloidal fineness. The silica, which is preferably amorphous, may be that obtained as a waste product from the production of ferro-silicon, or the natural, finely divided materials such as chalcedony, geyserite or diatomaceous earth, or rice hull ashes may be used; alternatively, it may be obtained by reducing relatively-pure siliceous material such as quartz by heating with carbon, allowing the silicon to reoxidise, and collecting the product. The magnesia may be the dust obtained by electrostatic precipitation or otherwise from the flue gases of furnaces for calcining magnesite, precipitated magnesia, particularly that obtained by the treatment of seawater or brine with lime or calcined dolomite, or powdered calcined magnesite or brucite. In order to convert any lime and iron present in the ingredients into monticellite and magnesioferrite respectively, a slight excess of magnesia is employed, the proportions being 60 MgO to 40 SiO2. The ingredients are mixed together with a small amount of water, and cold-setting bonds, such as waste sulphite liquor, tar, sulphite pitch, molasses, or magnesium chloride or sulphate, may be incorporated. If magnesium precipitated from brine is employed, the mixture of the ingredients may be prepared by adding the finely-divided silica to the brine either before or after treatment with the lime. After mixing, the product may be shaped if desired, and the mixture is finally burnt at approximately 1450 DEG C., or clinkers may be produced which are subsequently ground and bonded by the same or a different material. Specifications 579,098 and 602,454, and U.S.A. Specifications 852,908 and 1,659,476 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US602453XA | 1944-04-21 | 1944-04-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB602453A true GB602453A (en) | 1948-05-27 |
Family
ID=22028283
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16958/44A Expired GB602453A (en) | 1944-04-21 | 1944-09-05 | Synthetic forsterite materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB602453A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2590566A (en) * | 1949-06-22 | 1952-03-25 | Harbison Walker Refractories | Hydrothermal synthesis of forsterite |
US4049780A (en) * | 1972-11-14 | 1977-09-20 | Laporte Industries Limited | Production of magnesium silicates |
GB2347143A (en) * | 1999-02-24 | 2000-08-30 | Brightcross Manufacturing Limi | Refractory composition |
CN109133949A (en) * | 2018-09-21 | 2019-01-04 | 山西通才工贸有限公司 | A kind of utilization method of magnesia waste material |
CN110713380A (en) * | 2019-11-28 | 2020-01-21 | 王衍森 | Preparation method of high-purity compact forsterite |
CN112321308A (en) * | 2020-11-25 | 2021-02-05 | 辽宁科技大学 | Preparation method of forsterite low-iron refractory homogeneous material |
CN112321290A (en) * | 2020-12-01 | 2021-02-05 | 牟春树 | Method for producing sintered forsterite |
CN113603105A (en) * | 2021-08-31 | 2021-11-05 | 西南科技大学 | Method for hydrothermally synthesizing serpentine from olivine at low temperature and low pressure and serpentine |
CN113897665A (en) * | 2021-11-09 | 2022-01-07 | 中国科学院地球化学研究所 | Preparation method of high-titanium and high-water-content forsterite single crystal |
-
1944
- 1944-09-05 GB GB16958/44A patent/GB602453A/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2590566A (en) * | 1949-06-22 | 1952-03-25 | Harbison Walker Refractories | Hydrothermal synthesis of forsterite |
US4049780A (en) * | 1972-11-14 | 1977-09-20 | Laporte Industries Limited | Production of magnesium silicates |
GB2347143A (en) * | 1999-02-24 | 2000-08-30 | Brightcross Manufacturing Limi | Refractory composition |
CN109133949A (en) * | 2018-09-21 | 2019-01-04 | 山西通才工贸有限公司 | A kind of utilization method of magnesia waste material |
CN110713380A (en) * | 2019-11-28 | 2020-01-21 | 王衍森 | Preparation method of high-purity compact forsterite |
CN112321308A (en) * | 2020-11-25 | 2021-02-05 | 辽宁科技大学 | Preparation method of forsterite low-iron refractory homogeneous material |
CN112321290A (en) * | 2020-12-01 | 2021-02-05 | 牟春树 | Method for producing sintered forsterite |
CN113603105A (en) * | 2021-08-31 | 2021-11-05 | 西南科技大学 | Method for hydrothermally synthesizing serpentine from olivine at low temperature and low pressure and serpentine |
CN113897665A (en) * | 2021-11-09 | 2022-01-07 | 中国科学院地球化学研究所 | Preparation method of high-titanium and high-water-content forsterite single crystal |
CN113897665B (en) * | 2021-11-09 | 2022-07-26 | 中国科学院地球化学研究所 | Preparation method of high-titanium and high-water-content forsterite single crystal |
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