GB580367A - Process for manufacture of magnesium products - Google Patents

Process for manufacture of magnesium products

Info

Publication number
GB580367A
GB580367A GB1890243A GB1890243A GB580367A GB 580367 A GB580367 A GB 580367A GB 1890243 A GB1890243 A GB 1890243A GB 1890243 A GB1890243 A GB 1890243A GB 580367 A GB580367 A GB 580367A
Authority
GB
United Kingdom
Prior art keywords
carbonate
magnesium
bicarbonate solution
solids
per cent
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
Application number
GB1890243A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Marine Magnesium Products Corp
Original Assignee
Marine Magnesium Products Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Marine Magnesium Products Corp filed Critical Marine Magnesium Products Corp
Priority to GB1890243A priority Critical patent/GB580367A/en
Publication of GB580367A publication Critical patent/GB580367A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F5/00Compounds of magnesium
    • C01F5/24Magnesium carbonates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

Neutral hydrated magnesium carbonate is precipitated by aerating a magnesium bicarbonate solution with a relatively inert gas, e.g., decarbonated air or natural gas, at a rate insufficient to cause violent agitation, removing the suspension of neutral carbonate and reintroducing solid magnesium carbonate in amounts substantially, e.g., four to six times, greater than the amounts being precipitated so as to produce large particles e.g., 150 microns. The bicarbonate solution may be obtained from brines, or by crushing and calcining magnesium materials, e.g., dolomite, prucite, magnesite, serpentine, olivine, preferably selectively leaving calcium carbonate largely undecomposed; grinding preferably wet to 200 mesh, forming a magnesium hydroxide slurry; pretreating during or after grinding with flue <PICT:0580367/III/1> gas or bicarbonate solution to convert calcium oxide to rapid settling carbonate; diluting to, e.g., three per cent. solids; carbonating at normal or increased pressure; removing solids, e.g., by a hydro-separator or centrifuge, and clarifying. Magnesium carbonate may be recovered from the sludge solids by a continuous stream of water. Carbonation may be carried out in a series of tanks, the pressure rising to 20lbs. per square inch. Enriched carbon dioxide or high pressure carbonation may be used. As shown 2.5 per cent. magnesium bicarbonate solution 65 is aerated under normal conditions of temperature and pressure in three tanks 51, 52, 53 fitted with perforated bottom plates and baffles and supplied with successively greater amounts of air 57. Pentahydrate is deposited below 15 DEG C. and trihydrate at 15-40 DEG C. The suspension passes to the hydraulic thickener 62 and then to a centrifuging or dewatering stage. Sufficient thickened slurry is returned 64 to the aeration stage to maintain a content of 6-10 per cent. neutral solids. The evolved carbon dioxide is recovered at 67 for reuse. Only about 55-65 per cent. of the bicarbonate is decomposed and residual bicarbonate solution from the thickening and centrifuging stages is recycled 66 to the precarbonation dilution stage and/or the pretreatment stage. The magnesium carbonate may be ignited to oxide or dried and expanded at 250-400 DEG C. to produce basic carbonate. Specification 529,127 is referred to.
GB1890243A 1943-11-12 1943-11-12 Process for manufacture of magnesium products Expired GB580367A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1890243A GB580367A (en) 1943-11-12 1943-11-12 Process for manufacture of magnesium products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1890243A GB580367A (en) 1943-11-12 1943-11-12 Process for manufacture of magnesium products

Publications (1)

Publication Number Publication Date
GB580367A true GB580367A (en) 1946-09-05

Family

ID=10120373

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1890243A Expired GB580367A (en) 1943-11-12 1943-11-12 Process for manufacture of magnesium products

Country Status (1)

Country Link
GB (1) GB580367A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2694620A (en) * 1951-06-02 1954-11-16 Canadian Refractories Ltd Recovery of magnesia
EP1009717A1 (en) * 1997-08-20 2000-06-21 Martin Marietta Magnesia Specialties Inc. WET MILLING OF Mg(OH) 2? SLURRY

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2694620A (en) * 1951-06-02 1954-11-16 Canadian Refractories Ltd Recovery of magnesia
EP1009717A1 (en) * 1997-08-20 2000-06-21 Martin Marietta Magnesia Specialties Inc. WET MILLING OF Mg(OH) 2? SLURRY
EP1009717A4 (en) * 1997-08-20 2002-06-19 Martin Marietta Magnesia WET MILLING OF Mg(OH) 2? SLURRY

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