GB667708A - Improvements in or relating to preparation of catalytic and adsorbent magnesia-containing materials - Google Patents
Improvements in or relating to preparation of catalytic and adsorbent magnesia-containing materialsInfo
- Publication number
- GB667708A GB667708A GB952/50A GB95250A GB667708A GB 667708 A GB667708 A GB 667708A GB 952/50 A GB952/50 A GB 952/50A GB 95250 A GB95250 A GB 95250A GB 667708 A GB667708 A GB 667708A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- alcoholate
- water
- alcohols
- insoluble
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/10—Magnesium; Oxides or hydroxides thereof
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F5/00—Compounds of magnesium
- C01F5/14—Magnesium hydroxide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Catalysts (AREA)
Abstract
Magnesium metal or an alloy thereof is reacted with anhydrous methyl or ethyl alcohol, if desired in the presence of a catalyst such as mercury, mercuric chloride, aluminium chloride or iodine, and the alcoholate so formed treated with a substantially water-insoluble alcohol, if desired in admixture with a petroleum distillate. Suitable water-insoluble alcohols are n-, secondary- and isobutyl alcohols, pentanol-1, -2, and -3, 2-methyl butanol-3 and -4, hexanol-1, -2 and -3, methyl pentanols, di-methyl butanols, and heptyl- and hexyl alcohols. Suitable petroleum distillates are those boiling in the range 200-500 DEG F. Methyl or ethyl alcohol liberated is removed for reuse by distillation from the higher alcoholate formed.ALSO:Magnesia is prepared by reacting magnesium metal or an alloy thereof with anhydrous methyl or ethyl alcohol, if desired in the presence of a catalyst such as mercury, mercuric chloride, aluminium chloride or iodine, treating the alcoholate so formed with a substantially water-insoluble alcohol, if desired in admixture with a petroleum distillate, and hydrolyzing the resultant substituted alcoholate with water, at say 100-200 DEG F. to form a slurry of magnesia, and a separable layer of the water-insoluble alcohol for reuse. Suitable water-insoluble alcohols are n-, secondary- and isobutyl alcohols, pentanol-1, -2 and -3, 2 methyl butanol-3 and -4, hexanol-1, -2 and 3, methyl pentanols, dimethyl butanols, and heptyl- and hexyl alcohols. Suitable petroleum distillates are those boiling in the range 200 DEG -500 DEG F. Methyl or ethyl alcohol liberated is removed for reuse by distillation from the higher alcoholate formed. Separation of the hydrolized mixture into two layers is effected at 70 DEG -200 DEG F., and the alcohol-hydrocarbon mixture is dried by p distilling off the water. Small quantities of said mixture separating from the distillate are returned to the main separator. The magnesia slurry may be dried, or mixed with say, ammonium molybdate or dichromate, dried, and activated at 850 DEG F. to produce catalysts. Where mercury is used as a catalyst in the first stage, it may be recovered by contacting the magnesium alcoholate solution prior to hydrolysis with copper or silver, which may be deposited on pumice, silica gel, alumina &c. and subsequently distilling at a temperature up to 1000 DEG F. Hydrogen evolved in the first reaction may be compressed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US667708XA | 1949-03-15 | 1949-03-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB667708A true GB667708A (en) | 1952-03-05 |
Family
ID=22071582
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB952/50A Expired GB667708A (en) | 1949-03-15 | 1950-01-13 | Improvements in or relating to preparation of catalytic and adsorbent magnesia-containing materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB667708A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997024304A2 (en) * | 1995-12-27 | 1997-07-10 | RWE-DEA Aktiengesellschaft für Mineraloel und Chemie | Process for the preparation of high-purity magnesium hydroxide and magnesium oxide from magnesium alkoxides |
EP1541541A1 (en) * | 2003-12-13 | 2005-06-15 | Degussa AG | Process for the preparation of pure alkaline earth alkoxides |
EP1541540A1 (en) * | 2003-12-13 | 2005-06-15 | Degussa AG | Process for the preparation of pure alkaline earth alkoxides |
-
1950
- 1950-01-13 GB GB952/50A patent/GB667708A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997024304A2 (en) * | 1995-12-27 | 1997-07-10 | RWE-DEA Aktiengesellschaft für Mineraloel und Chemie | Process for the preparation of high-purity magnesium hydroxide and magnesium oxide from magnesium alkoxides |
WO1997024304A3 (en) * | 1995-12-27 | 1997-08-14 | Rwe Dea Ag | Process for the preparation of high-purity magnesium hydroxide and magnesium oxide from magnesium alkoxides |
US6569399B2 (en) | 1995-12-27 | 2003-05-27 | Sasol Germany Gmbh | Process for the preparation of high-purity magnesium hydroxide and magnesium oxide from magnesium alkoxides |
EP1541541A1 (en) * | 2003-12-13 | 2005-06-15 | Degussa AG | Process for the preparation of pure alkaline earth alkoxides |
EP1541540A1 (en) * | 2003-12-13 | 2005-06-15 | Degussa AG | Process for the preparation of pure alkaline earth alkoxides |
JP2005170947A (en) * | 2003-12-13 | 2005-06-30 | Degussa Ag | Process for preparation of alkoxy-pure alkaline earth alkoxide |
US7423186B2 (en) | 2003-12-13 | 2008-09-09 | Degussa Ag | Process for preparing alkoxy-pure alkaline earth alkoxides |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1515620A (en) | Continuous production of alkyl acrylates free from ether | |
US2579251A (en) | Manufacture of aluminum alkoxides | |
US4016208A (en) | Acid production | |
JPS6125694B2 (en) | ||
GB667708A (en) | Improvements in or relating to preparation of catalytic and adsorbent magnesia-containing materials | |
US1931858A (en) | Production of unsaturated ethers | |
Hennion et al. | Reactions of α-Ketols Derived from Tertiary Acetylenic Carbinols. I. Preparation and Low Pressure Hydrogenation1 | |
US2932665A (en) | Preparation of nu, nu-diethyltoluamides | |
JPH0710811A (en) | Production of dialkyl carbonate | |
Fleck et al. | Stability of DDT and related compounds | |
BARKENBUS et al. | The preparation and properties of some tert-alkyl formates | |
GB2033387A (en) | Production of di-n-propyl-acetic acid | |
US3657365A (en) | Process for the manufacture of methyl or ethyl chloride from methyl or ethyl acetate | |
US2464244A (en) | Production of methyl vinyl ketone | |
JPS6032740A (en) | Production of o-benzylphenol | |
IE43389B1 (en) | Process for the addition of organic acids to acetylenic compounds | |
WO2019069321A1 (en) | An improved process for the preparation of a key intermediate of gemfibrozil | |
US3734970A (en) | Preparation of methyl-beta-phenyl-ethyl-ether | |
US3173958A (en) | Ethers of olefin alcohols | |
GB727074A (en) | Manufacture of monochloroacetic acid | |
SU144167A1 (en) | Method for producing methyl isopropyl ketone | |
US3979432A (en) | Preparation of nitriles | |
US2019754A (en) | Preparation of organic acids | |
JP2782883B2 (en) | Method for producing tertiary olefin | |
SU119872A1 (en) | The method of obtaining beta-perfluoroalkoxy-1,1-dihydroperfluoropropyl alcohol |