CA1242750A - Preparation of dimethyl ether by catalytic dehydration of methanol - Google Patents

Preparation of dimethyl ether by catalytic dehydration of methanol

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Publication number
CA1242750A
CA1242750A CA000460655A CA460655A CA1242750A CA 1242750 A CA1242750 A CA 1242750A CA 000460655 A CA000460655 A CA 000460655A CA 460655 A CA460655 A CA 460655A CA 1242750 A CA1242750 A CA 1242750A
Authority
CA
Canada
Prior art keywords
methanol
dimethyl ether
preparation
alumina
catalyst
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
CA000460655A
Other languages
French (fr)
Inventor
Loren D. Brake
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to CA000460655A priority Critical patent/CA1242750A/en
Application granted granted Critical
Publication of CA1242750A publication Critical patent/CA1242750A/en
Expired legal-status Critical Current

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Abstract

PREPARATION OF DIMETHYL ETHER
BY
CATALYTIC DEHYDRATION OF METHANOL
ABSTRACT OF THE DISCLOSURE
In the preparation of dimethyl ether by the catalytic dehydration of methanol, reaction rate is enhanced and catalyst coking and byproduct formation are significantly reduced when an aluminotitanate containing 0.5-20% of titania and 80-99.5% of alumina is used as the catalyst.

Description

'7~

PREPARATION OF DIMETHYL ETHER
BY
CATALYTIC DEHYDRATION OF METHANOL

DESCRI PT ION

Technical Field This invention relates to an impro~7ed method for the preparation of dimethyl ether by the catalytic dehydration of methanol. It is more par-ticularly directed to such a method in which the catalyst used is an aluminotitanate.

15 Background and Summary of the Invention Dimethyl ether is a commodity in the chemi-cal industry, widely used as A starting material in the preparation of other chemicals such as dimethyl sulfate, and more recently as a propellant in aerosol containers.
One of the commonly used methods for pre-paring dimethyl ether is the catalytic dehydration of methanol, ~sing a phosphoric acid-alumina catalystO
While that process is generally satisfactory, the catalyst has a tendency to coke, which requires it to be replaced more frequently than is desirable. By "coke" is meant the phenomenon by which the surface of the catalyst becomes coated with carbon, thus blocking its pores and reducing its effectiveness.
It has now been found that this coking can be minimized if~ instead of the phosphoric acid-alumina catalyst, one uses an aluminotitanate cata-lyst containing 0.5-20~ by weight of titania and 80-99.5% by weight of gamma-alumina~ Surprisingly, CH-1265 35 use of such a catalyst not only reduces the amount of ~2~7r3~
coking but also significantly increases the rate of the dehyration reaction over that obtained with the phosphoric acid-alumina catalyst, and greatly reduces the number and amounts of byproducts formed, notably hydrogen, carbon monoxide, methane, ethane, propane, ethylene, propylene and various ethers having high boiling points.

Detailed Description of the Inv_n ion The catalytic dehydration of methanol to form dimethyl ether is well known and is described in detail in U.S. Patent 2,014,408 to John C. WoodhouseO
The reaction proceeds according to the general equation 2CH30H ~ CH30CH3 + H2O

The product of the reaction is a mixture principally containing dimethyl ether, unreacted methanol and water~
The reaction is ordinarily conducted con-tinuously in a column reactor, in the vapor phase, generally at a maximum reactor bed temperature of200-500C, preferably 275-420~C, and a pressure ranging from ambient to 3447 kPa (gauge), preferably 1034-1723 kPa (gauge). The catalyst is packed into the reactor in the customary way, and the vaporized and preheated (200-300C) methanol is passed through it, preferably downwardly.
Residence time of the methanol in the reactor is selected according to well-known chemical 5~

engineering principles, as are the methods of re-covering the dimethyl et~er from the reactor effluent and the methods of refining it.
The catalysts used according to the inven-tion are aluminotitanates containing 0.5-20~ by weight of titania and 80-9~.5% by weight of gamma alumina, perferably 0.5-10% of titania and 90-9~.5~
of alumina, even more preferably about 1% of titania and about 99% of alumina.
The catalysts can contain the titania dis-tributed throughout the alumina, i.e., they can be homogeneous catalysts, or they can contain the titania as a coating on the alumina.
The homogeneous catalysts can be made by mixing aqueous solutions of TiC14 and sodium alumi-nate, in proportions precalculated to give the de-sired titania/alumina ratio, and then bringing the solution to a pH of about 8 with hydrochloric acid, at a temperature of 50~70C. The resulting gel, a ~ mixture of hydroxides, is recovered~ washed free of chlorides with water, dried to a free-flowing pow~er, shaped and then calcined at 450-650C to give a mate-rial which can be used directly as the catalyst.
The catalyst of alumina coated with titania 2S can be ma~e by first preparing a pourable aqueous slurry oE boehmite or gamma alumina powder and then adding to it, with vigorous stirriny, an aqueous 10-20% by weight solution of TiC14, in proportions precalculatd to give the desired alumina-titania ratio. The slurry is then adjusted to a p~ of about 3 with NaOH and is held for 30 minutes, with stirring, at 50-70C. The solids are then removed by filtration or centrifugation, dried to a free-flowing powder, shaped and then calcined at 500-550C.

~ 2L~2~7S~3 The catalyst is generally used as shaped forms, ordinarily pellets or spheroids. Form size is selected according to recognized chemical engineering principles, and is usually in the range 2-120 mm in all dimensions. The pore volume, pore size and total surface area of the forms are likewise a matter of choice, and will generally be in the range of 0~2-0~8 cc/g, greater than 25 angstrom units, and 100-25U
m2/g, respectively.

EXA~PLE
In the following example, all parts are by weight Forty-five parts of an nomogeneous alumino-titanate containing about 99~ of gamma alumina and about 1~ of ~itania, in the form of spheroids having diameters of 3.15 mm, were mixed with 319 parts of glass spheroids having diameters of 4 mm.
The mixture was packed into a column reactor having a length/diameter ratio of 4.
Methanol, preheated to 300C, was then con-tinuously fed into the top of the reactor. The vapors were passed downwardly through the catalyst bed at the rate of 660 parts per hour. Pressure in the reactor was held at 1034 kPa (gauge); the reactor bed temperature reached a maximum of 400C.
The vapors leaving the reactor were con-densed to give a product having the average composition Dimethyl ether 57.5 ~lethanol 20%
Water 22.5

Claims (4)

1. In the preparation of dimethyl ether by the catalytic dehydration of methanol, the improvement which comprises using as the catalyst an aluminotitanate which contains, by weight, 0.5-20% of titania and 80-99.5% of alumina.
2. The process of Claim l in which the catalyst contains 0.5-10% of titania and 90 99.5% of alumina.
3. The process of Claim 1 in which the catalyst contains about 1% of titania and about 99% of alumina.
4. In the preparation of dimethyl ether by the catalytic dehydration of methanol, the improvement which comprises using the catalyst which comprises gama-alumina bearing a coating of about 1%, by weight, of titania.
CA000460655A 1984-08-09 1984-08-09 Preparation of dimethyl ether by catalytic dehydration of methanol Expired CA1242750A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA000460655A CA1242750A (en) 1984-08-09 1984-08-09 Preparation of dimethyl ether by catalytic dehydration of methanol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA000460655A CA1242750A (en) 1984-08-09 1984-08-09 Preparation of dimethyl ether by catalytic dehydration of methanol

Publications (1)

Publication Number Publication Date
CA1242750A true CA1242750A (en) 1988-10-04

Family

ID=4128499

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000460655A Expired CA1242750A (en) 1984-08-09 1984-08-09 Preparation of dimethyl ether by catalytic dehydration of methanol

Country Status (1)

Country Link
CA (1) CA1242750A (en)

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