CN101024599A - Solid magnesium ethoxide and preparing method - Google Patents
Solid magnesium ethoxide and preparing method Download PDFInfo
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- CN101024599A CN101024599A CN 200710065115 CN200710065115A CN101024599A CN 101024599 A CN101024599 A CN 101024599A CN 200710065115 CN200710065115 CN 200710065115 CN 200710065115 A CN200710065115 A CN 200710065115A CN 101024599 A CN101024599 A CN 101024599A
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- magnesium ethoxide
- solid magnesium
- iodine
- ethoxide
- powder
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Abstract
The invention relates to solid magnesium ethoxide and the manufacturing method. It includes the following steps: using absolute ethyl alcohol and high purity metal magnesium powder as raw material, adding little iodine as catalyst, whisking equal and heating, adding catalyst to take reaction, pouring the solution into drier after reacting, heating to vaporizing alcohol and drying in vacuum to gain solid magnesium ethoxide. The constituents includes: iodine 0.8-1.2, metal magnesium powder 10-16, and absolutely alcohol 300-600. The benefit of the invention is that the content of magnesium ethoxide is high, and other element is low, it could replace liquid magnesium ethoxide to improve reacting yield and product quality, and decrease energy consumption. The vaporized alcohol could be used to compound other products or fully recycled. Thus, the resource would be saved.
Description
Technical field
The present invention relates to a kind of solid magnesium ethoxide and preparation method, belong to metal compound preparation technical field.
Background technology
Solid magnesium ethoxide is the nontoxic medicine source material of a kind of solid magnesium ethoxide and preparation method, indispensable catalyzer series products such as PPA, methoxy Bian pyrimidine main raw material, plastics, spices, essence, makeup, agricultural chemicals.
Summary of the invention
In order to overcome the deficiencies in the prior art, the invention provides a kind of solid magnesium ethoxide and preparation method.
The technical solution adopted for the present invention to solve the technical problems is: the operational path of employing is as main raw material with dehydrated alcohol and high-purity magnesium metal powder, add a small amount of iodine again and make catalyzer, the catalyzed reaction of heating after fully stirring, after finishing, reaction injects a solution in the moisture eliminator, heating steams the back to ethanol in vacuum-drying, thereby obtains solid magnesium ethoxide.The part by weight of prescription is:
Iodine 0.8-1.2 metal magnesium powder 10-16 dehydrated alcohol 300-600;
Get metal magnesium powder, dehydrated alcohol and iodine according to the above ratio, fully mix up, begin to heat, temperature is reacted between 60-90 ℃, after reaction finishes, injects a solution in the moisture eliminator, heat ethanol is steamed vacuum-drying again, dryer temperature is about 90-150 ℃, and the ethanol that steams returns use, just obtains solid magnesium ethoxide after drying finishes.
A kind of solid magnesium ethoxide and preparation method comprise the steps:
1, dehydrated alcohol adds metal magnesium powder and adds iodine again, after fully stirring, heats and carries out the synthesis catalytic reaction.
2, after building-up reactions finishes, material is injected in the moisture eliminator, heat and distill vacuum-drying, all other reclaims distillation centrifugal ethanol except that synthetics, and the solution that returns can be used again.
Beneficial effect of the present invention;
The solid magnesium ethoxide major advantage is a magnesium ethylate content height, and it is extremely low that free ethanol and other contain thing, substitutes the liquid magnesium ethylate, can improve reaction yield and quality product, reduces the energy simultaneously.Solid magnesium ethoxide is to intend white, powdery and granular.After building-up reactions finishes, material is injected in the moisture eliminator, heat and distill vacuum-drying, all other reclaims distillation centrifugal ethanol except that synthetics, and the solution that returns can be used again, economizes on resources.
Solid magnesium ethoxide mainly acts on medicine source material, as PPA, methoxy Bian pyrimidine, and catalyzer such as the catalyzer of processing fat and edible oil, plastics catalyzer, spices, essence, makeup, agricultural chemicals.
Description of drawings
Fig. 1 is a process flow diagram.
Below in conjunction with drawings and Examples invention is further specified.
Embodiment
Embodiment 1: the part by weight of prescription is:
Iodine 0.8 metal magnesium powder 10 dehydrated alcohols 300;
Technical process as shown in Figure 1, get metal magnesium powder, dehydrated alcohol and iodine according to the above ratio, fully mix up, begin to heat, temperature is reacted between 60 ℃, after reaction finishes, inject a solution in the moisture eliminator, heating steams vacuum-drying again to ethanol, and dryer temperature is about 90 ℃, the ethanol that steams returns use, just obtains solid magnesium ethoxide after drying finishes.
Embodiment 2: the part by weight of prescription is:
Iodine 1.2 metal magnesium powders 16 dehydrated alcohols 600;
Get metal magnesium powder, dehydrated alcohol and iodine according to the above ratio, fully mix up, begin to heat, temperature is reacted (as 90 ℃) between 60 ℃-90 ℃, after reaction finishes, inject a solution in the moisture eliminator, heat ethanol is steamed vacuum-drying again, dryer temperature is about 90 ℃-150 ℃ (as 150 ℃), and the ethanol that steams returns use, just obtains solid magnesium ethoxide after drying finishes.
Embodiment 3: the part by weight of prescription is:
Iodine: metal magnesium powder: the alcoholic acid ratio is 1: 15: 525;
Get metal magnesium powder, dehydrated alcohol and iodine according to the above ratio, fully mix up, begin to heat, temperature is reacted (as 50 ℃) between 50 ℃-90 ℃, after reaction finishes, inject a solution in the moisture eliminator, heat ethanol is steamed vacuum-drying again, dryer temperature is about 80 ℃-140 ℃ (as 140 ℃), and the ethanol that steams returns use, just obtains solid magnesium ethoxide after drying finishes.
The above, it only is preferred embodiment of the present invention, be not that the present invention is done any pro forma restriction, though the present invention enumerates as above with preferred embodiment, yet be not in order to limit the present invention, any those skilled in the art, in not breaking away from the technical solution of the present invention scope, when utilizing the above-mentioned technology contents of enumerating to make a little change or being modified to the equivalent embodiment of equivalent variations, in every case be the content that does not break away from technical solution of the present invention, according to technical spirit of the present invention to any simple modification that above embodiment did, equivalent variations and modification all still belong in the scope of technical solution of the present invention.
Claims (5)
1. the preparation method of a solid magnesium ethoxide, it is characterized in that: with dehydrated alcohol and high-purity magnesium metal powder as main raw material, add a small amount of iodine again and make catalyzer, the catalyzed reaction of heating after fully stirring, after finishing, reaction injects a solution in the moisture eliminator, heating steams the back to ethanol in vacuum-drying, thereby obtains solid magnesium ethoxide.The part by weight of prescription is: iodine 0.8-1.2 metal magnesium powder 10-16 dehydrated alcohol 300-600.
2. the preparation method of a kind of solid magnesium ethoxide according to claim 1, it is characterized in that: get metal magnesium powder, dehydrated alcohol and iodine in described ratio, fully mix up, begin to heat, temperature is reacted between 60-90 ℃, after reaction finishes, inject a solution in the moisture eliminator, heating steams vacuum-drying again to ethanol, and dryer temperature is about 90-150 ℃, the ethanol that steams returns use, just obtains solid magnesium ethoxide after drying finishes.
3. the preparation method of a kind of solid magnesium ethoxide according to claim 1 and 2, it is characterized in that: the part by weight of prescription is:
Iodine: metal magnesium powder: the alcoholic acid ratio is 1: 15: 525.
4. solid magnesium ethoxide is characterized in that: the solid magnesium ethoxide of making according to claim 1 or 2 described methods.
5. solid magnesium ethoxide is characterized in that: the solid magnesium ethoxide of making according to the described method of claim 3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN 200710065115 CN101024599A (en) | 2007-04-04 | 2007-04-04 | Solid magnesium ethoxide and preparing method |
Applications Claiming Priority (1)
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CN 200710065115 CN101024599A (en) | 2007-04-04 | 2007-04-04 | Solid magnesium ethoxide and preparing method |
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CN101024599A true CN101024599A (en) | 2007-08-29 |
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CN 200710065115 Pending CN101024599A (en) | 2007-04-04 | 2007-04-04 | Solid magnesium ethoxide and preparing method |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102898279A (en) * | 2012-10-19 | 2013-01-30 | 北京理工大学 | Preparation method for solid metal alkoxide |
CN104447203A (en) * | 2015-01-09 | 2015-03-25 | 铜陵金泰化工股份有限公司 | Synthetic method of potassium ethylene glycol |
CN107098794A (en) * | 2017-05-18 | 2017-08-29 | 山西大学 | A kind of preparation method of solid magnesium ethoxide |
-
2007
- 2007-04-04 CN CN 200710065115 patent/CN101024599A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102898279A (en) * | 2012-10-19 | 2013-01-30 | 北京理工大学 | Preparation method for solid metal alkoxide |
CN102898279B (en) * | 2012-10-19 | 2014-10-15 | 北京理工大学 | Preparation method for solid metal alkoxide |
CN104447203A (en) * | 2015-01-09 | 2015-03-25 | 铜陵金泰化工股份有限公司 | Synthetic method of potassium ethylene glycol |
CN107098794A (en) * | 2017-05-18 | 2017-08-29 | 山西大学 | A kind of preparation method of solid magnesium ethoxide |
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Open date: 20070829 |