NO783833L - PROCEDURE FOR THE PREPARATION OF UNSaturated Acids - Google Patents

Description

Methacrylic acid or acrylic acid is produced according to the invention by oxidation of methacrolein, respectively. acrolein, with molecular oxygen in the vapor phase in the presence of a catalytic oxide of molybdenum, phosphorus, arsenic, oxygen and the following constituents. indicated in three

groups I to III: (I) a rare earth element or mixture thereof, and possibly at least one of Ag, Tl, Rh, Pd, Ru, Pt, Cd, Al, Au, Cu, alkaline earth metal, Cl and NH^; or (II) at least one element selected from the group consisting of U, Ti, Nb, Re, Pb, Zn and Ga, and optionally at least one of Cu, a rare earth element, Ag, Ta, In, Th, Cd, Tl, alkaline earth metal , NH 3 , Cl, Ni, Al and Ge; or (III) at least one element selected from the group consisting of Ag, Rh, Ru and Au, and optionally at least one of Cd, Pt, Tl, Pd, Al, Ge, Cu, Ni, alkaline earth metal, NH^ and Cl.

A number of catalysts are known to be effective for the oxidation of acrolein or methacrolein to acrylic acid, respectively. methacrylic acid. However, the yields obtained using the catalysts for the production of methacrylic acid are low. DT patent 2 0^8 620 relates to catalysts containing the oxides of molybdenum, phosphorus and arsenic for the oxidation of methacrolein and acrolein to methacrylic acid, respectively. acrylic acid. U.S. patent no. 3 761 516 relates to catalysts containing oxides of molybdenum, arsenic and phosphorus on a support, in particular. A120, with external macro-pores and a surface not greater than 2 m2/g.

The present invention is the result of a search for more effective and desirable catalysts for the production of acrylic acid and methacrylic acid. Unexpectedly higher yields of and selectivities for acrylic acid and methacrylic acid are obtained by vapor phase oxidation of acrolein, resp. methacrolein, with molecular oxygen in the presence of the new and useful catalysts according to the present invention.

It has been shown that according to the present invention in the method for the production of acrylic acid or methacrylic acid by oxidation of acrolein, resp. methacrolein, with molecular oxygen in the vapor phase at a reaction temperature of from approx. 200°C to approx. 500°C in the presence of. an oxide catalyst, and optionally in the presence

of steam, the improvement characterized by the use of a catalyst with the formula:

where X is a rare earth element or a mixture thereof; U is at least one of Ag, Tl, Rh, Pd, Ru, Pt, Cd, Al, Au, Cu, alkaline earth metal, Cl and NH^; where a is 0.001 to 10; b.is 0 to 10; c is 0.01 to 5; d is 0.01 to 5; x is the number of oxygen atoms required to satisfy the valence states of the other elements present; or that a catalyst with the formula is used: where X is at least one element selected from the group consisting of U, Ti, Nb, Re, Pb, Zn and GA; Y is Cu, a rare earth element, Ag, Ta, In, Th, Cd, Tl, an alkaline earth metal, NH^, Cl, Ni, Al and Ge; and where a is 0.001 to 10; b is 0 to 10; c is 0.01 to 5; d is 0.01 to 5; x is the number of oxygen atoms required to satisfy the valence states of the other elements present; or a catalyst with the formula is used:

where X is at least one element selected from the group consisting of Ag, Rh, Ru and Au i

Y is at least one of Cd, Tl, Pd, Al, Ge, Cu, Pt, Ni, alkaline earth metal, NH^ and Cl;

and where a is 0.001 to 10;

b is 0 to 10;

c is 0.01 to 5;

d is 0.01 to 5;

x is the number of oxygen atoms required to satisfy the valence states of the other elements present.

The surprisingly advantageous catalysts according to the invention provide improved yields of acrylic acid and methacrylic acid from acrolein, respectively. methacrolein, in an efficient, convenient and economical way at a relatively low temperature. The exotherm of the reaction is low, which enables easy reaction ion counter roll.

The most significant feature of the present invention is the catalyst used. The catalyst may be any of the catalysts indicated by formulas I to III. The catalysts can be prepared by a number of different known methods, such as coprecipitation of soluble salts and calcination of the product formed. The catalysts according to the invention have preferred restrictions on their composition.

When catalysts of formula I are used, preferred catalysts are those where a is 0.001 to 3>catalysts where b is 0.001 to 3>and catalysts where b is 0. Particularly preferred are catalysts where X is cerium, erbium or a mixture of rare earth elements consisting essentially of Ce, La, Nd and Pr. Catalysts of particular interest' are those where Y is silver, thallium or copper.

When catalysts of formula II are used, catalysts where a is 0.001 to 3, catalysts where b is 0.001 to 3 are preferred; and catalysts where b is 0. Particularly preferred are catalysts where each of the elements denoted by X is incorporated

separately in the catalyst. This is conveniently achieved by setting

X independently equals the different elements. Catalysts of particular interest are those where Y is at least one element selected from the group consisting of a rare earth element, Al, Ag and Cu.

When catalysts with formula ill are used, preferred catalysts are those where a is 0.001 to 3, catalysts where b is 0.001 to 3, and catalysts where b is 0. Particularly preferred are catalysts where each of the elements indicated by X is incorporated separately into the catalyst. This is conveniently achieved by setting X independently equal to the various elements. Also preferred are catalysts where Y is at least one of Cd, Tl, Cu, NH 4 and Cl.

In catalyst production, the different elements of the catalyst are combined, and the final product is calcined to obtain the catalyst. A number of methods for combining the elements of the catalyst and calcining the resulting product are known to those skilled in the art. For the broad idea of the invention, the particular method for producing the catalysts is not critical.

There are, however, methods for producing the catalysts which have been shown to be preferred. A preferred method involves preparing the catalysts in an aqueous slurry or solution of molybdenum, arsenic and/or phosphorus containing ingredients, and adding the remaining ingredients; evaporate this aqueous mixture and calcine the catalysts obtained. Suitable molybdenum compounds which can be used in the preparation of the catalysts indicated by the above formulas include molybdenum trioxide, phosphormolybdic acid, molybdic acid, ammonium heptamolybdate and the like. Suitable phosphorus compounds which can be used in the preparation of the catalysts include orthophosphoric acid, metaphosphoric acid, triphosphoric acid and phosphorus halides or oxyhalides. The remaining components of the catalysts can be used, such as oxide, acetate, formate, sulphate, nitrate, carbonate, oxyhalide or halide and the like.

Excellent results are obtained by refluxing phosphoric acid, an arsenic-containing compound and molybdenum trioxide or ammonium heptamolybdate in water for approx. half an hour to 3 hours, but commercial phosphormolybdic acid can be used effectively; adding the remaining ingredients to the aqueous slurry and boiling to a thick paste; drying at 110 - 120°C in air;

and calcination of the obtained catalysts.

The calcination of the catalyst is usually carried out by heating the dry catalytic components at a temperature of approx. 200°C to approx. 700°C. The preferred method according to the invention is the one where the catalyst is calcined at a temperature of 325 - 425°C.

The reactants in the reaction according to the invention are methacrolein or acrolein and oxygen. Molecular oxygen is usually supplied to the reaction in the form of air, but oxygen gas can also be used. About. 0.5 to approx. 4 mol of oxygen are usually added per moles of methacrolein.

The reaction temperature can vary according to which different catalysts are used. A temperature of approx.

200 to approx. 500°C, with a temperature of 250 - 370°C being preferred.

The catalyst can be used alone, or a carrier can be used. Suitable carriers include silicon oxide, aluminum oxide, "Alundum", silicon carbide, boron phosphate, zirconium dioxide and titanium dioxide. The catalysts are often used in a fixed-bed reactor such as tablets, pellets or the like, or in a suspended-bed reactor using a catalyst with a particle size of less than approx. 300 µm. When a fluidized bed reactor is used, the preferred catalysts are in the form of microspherical particles. The contact time can be as low as a fraction of a second or as high as 20 seconds or more. The reaction can be carried out at atmospheric pressure, overpressure or underpressure, with absolute pressures of approx. 0.5 to approx. 4 ata is preferred.

Excellent results are obtained using a coated catalyst consisting essentially of an inert support material with a diameter of at least 20 µm and having an outer surface and a continuous coating of the active catalyst on the inert support strongly adhering to the outer surface of the support . The special coated catalyst consists of an inner support material with an outer surface and a coating of active catalytic material

on this outer surface. These catalysts can be prepared by a number of different methods.

Carrier food eria light for catalyst, forms the inner core of the catalyst. This is a substantially inert carrier and can be of virtually any particle size although a diameter greater than 20 µm is preferred. Particularly preferred according to the present invention for use in a commercial reactor are the carriers which are spherical and have a diameter of from approx. 0.2 cm to approx. 2 cm. Suitable examples of substantially inert carrier materials include: "Alundum", silicon oxide, aluminum oxide, aluminum oxide-silicon oxide, silicon carbide, titanium dioxide and zirconium dioxide. Particularly preferred among these carriers are "Alundum", silicon oxide, aluminum oxide and aluminum oxide-silicon oxide.

The catalysts can contain virtually any ratio of carrier and catalytically active material. The limits of this relationship are set only by the relative ability of the catalyst and support material to adapt to each other. Preferred catalysts contain approx. 10 to approx. 100% by weight catalytically active material calculated on the weight of the carrier.

The production of these coated catalysts can be carried out by different methods. The basic method for producing these catalysts is to partially wet the carrier material with a liquid and then bring the carrier material into contact with a powder of the catalytically active material and gently shake the mixture until the catalyst is formed. The gentle shaking is most conveniently accomplished by placing the partially wet support in a rotating drum or jar and adding the powdered active catalytic material.

When using the catalysts according to the invention in the production of methacrylic acid or acrylic acid, excellent yields are obtained in a convenient reaction with low amounts of by-products.

Specific embodiments

Comparative examples A to D and examples 1 to 80: Comparison of catalysts containing promoters according to the invention with basic catalyst in the production of methacrylic acid.

A 20 cm 3 fixed lid reactor was constructed from a 1.3 cm stainless steel tube.. Catalysts prepared . as described above,

was introduced into the reactor and heated to the reaction temperature under an air stream and a feed of methacrolein/air/nitrogen/steam in the ratio 1:5.7:4.6:8.7 was fed over the catalyst with an apparent contact time of 2 - 4 seconds. The reactor was run under the reaction conditions for 1-6 hours, and the product was collected and analyzed.

Comparative example A

25% Mo12PiAso 5°x + 75% "Alundum"

A solution was prepared consisting of 211.88 g of ammonium heptamolybdate, (NH^)gMo^^. 4h 2 O , (1.2 mol Mo), 500 ml distilled

water of 6o°C and 7.94 g of ammonium arsenate, NH^H2AsO^ (0.05 mol As) as a solution in 25 ml of distilled water. A white precipitate was formed

formed which was heated to approx. 100°C for 2 hours. 11.53985% phosphoric acid (0.10 mol P) was added to this mixture. Half an hour later, 5.0 g of hydrazine hydrate was added. The slurry was evaporated to a thick paste, dried overnight in an oven at 110 - 120°C and ground and screened to less than 80 mesh. This powder was coated on "Norton. 3.2 mm SA 5223" "Alundum" beads by partially wetting 50 g of "Alundum" with 1.8 g of water and adding 16.7 g of active catalyst prepared above in five equal portions . During and after each addition, the "Alundum" balls were rolled in a glass jar. The powder was uniformly coated on the surface of the "Alundum" balls and the final product was dried. A hard, uniform material was obtained which consisted of an inner core of the "Alundum" carrier with a continuous, highly adherent coating of the powder on the outer surface of the carrier. The material was then calcined for 1 hour at 370°C in 40 ml/min air to form the active catalyst.

Examples 1 to 9

Various catalysts of formula I were prepared as follows:

Example 1

<25%>(rare earth mixture)Qi25Mo12P1As0 ^0y<+>75% "Alundum"

A solution was determined consisting of 105.9 g of ammonium heptamolybd (NH 2 ) gMo 2 . 4^0, (0.6 mol Mo), 700 ml distilled water at 60 C and 4.0 g ammonium a r senate , NH^AsO^, (0.025 mol As)

as a solution in 25 ml of water. A white precipitate was formed which was heated at 100°C for half an hour. To this mixture was added 4.4 g of Moly Corp. rare earth chloride mixture (product -

code no. 4700) consisting of 48% Ce02, 33% La^', 13% Nd20,

4.5% Pr601 and 1.5% other rare earth elements calculated as oxides. To this solution was added 5.8 g of 85% phosphoric acid, H3PO4(°'°5 mo1 P) - Half an hour later, 2.5 g of hydrazine hydrate was added. The slurry was evaporated to a thick paste,

dried overnight in an oven at 110 - 120°C and ground and sieved to below 80 mesh size. The catalyst was then coated to an active thickness of 25% on 3.2 mm "SA 5223" "Alundum" beads. Calcination was the same as in Comparative Example A.

Example 2 to 7

Preparation of the catalysts

25% X Y.Mo., „P.. As_ -0 + 75% "Alundum"

a. b 12 1 Oo x

Various catalysts according to the invention were prepared. The catalysts were prepared according to the method in example 1 using 105.9 g of ammonium molybdate, 700 ml of 60°C distilled water and 4.0 g of ammonium arsenate dissolved in 25 ml of water. The catalytic components indicated by X and/or Y were added immediately before the addition of 5.8 g of 85% phosphoric acid and 2.5 g of hydrazine hydrate. To prepare the catalysts, the following compounds and amounts were used:

Example 8

25% rare earth metal mixture ' 0t-O-U nCMon „P,As„ r0

u,<o 0.03 12 1 0.5 x

+ 75% "Alundum"

This catalyst was prepared in the same manner as described in Example 1, except that 34.25 g of ammonium heptamolybdate, 1.28 g of ammonium arsenate, 1.43 g of rare earth chloride mixture,

0.161 g of copper acetate<:>, 1.88 g of 85% phosphoric acid and 0.8 g of hydrazine hydrate were used.

Example 9

25% rare earth metal mixture0 2^ Ago lM°l2PlAs0 5°x<+>75% " Alundum"

This catalyst was prepared in the same manner as described in Example 8, except that 0.269 g of silver acetate was used.

Comparative examples B, C and examples 10 to 20

The results of the experiments using catalysts of formula I in the oxidation of methacrolein to produce methacrylic acid are shown in Table I. The following definitions are used to measure the carbon atoms in the feed and products.

Examples 21 to 43

Various catalysts of formula II were prepared as follows:

Example 21

2<5%>UQ 25Moi2PiAso 5°x + 75% "Alundum"

A solution was prepared consisting of 105.9 g of ammonium heptamolybdate, (NH^) 6Mo^O2^-4H20, (0.6 mol Mo), 700 ml of distilled water at 6o°C and 4.0 g of ammonium arsenate, NH^H2AsO^ (0.025 mol As) dissolved in 25 ml of water. A white precipitate was formed which was heated at 100°C for approx. half hour. To this mixture was added 5.3 g uranyl acetate (0.0125 mol U), followed by the addition of 5.8 g 85% phosphoric acid (0.05 mol P). Half an hour later, 2.5 g of hydrazine hydrate was added. The slurry was evaporated to a thick paste, dried overnight in an oven at 110 - 120°C and ground and sieved to below 80 mesh size. The catalyst was then coated to a 25% activity level on 3.2 mm "SA 5223" "Alundum" beads. The calcification was the same as in comparative ex-

pile A .

Example 22

25% TiQ 2Moi2PlAs0 5°x + 75% "Alundum"

This catalyst is prepared in the same way as described in example 21, except that 7.72 g of 20% titanium trichloride solution was used and hydrazine hydrate was looped at catalyst advance 11 - none.

Example 23

25% (rare earth metal mixture)^ 0T.i_ nMol0PnAs^ c0

+ 75% "Alundum" ■ 0, 2 0 , 1 12 1 0 , 5 x

This catalyst was prepared in the same way as described

in Example 21, except that 3.54 g of rare earth chloride mixture, 0.5 g of hydrazine hydrate were used, and 3.85 g of 20% titanium trichloride solution was added.

Examples 24 to 39

Preparation of the catalysts 25% X Y,Mo10PnAs^ c0 + 75% "Alundum"

: a dx<il o ,jx

Various catalysts according to the invention were prepared. The catalysts were prepared by the method in example 21, using 105.9 g of ammonium molybdate, 700 ml of distilled water at 60°C and 4.0 g of ammonium arsenate dissolved in 25 ml of water. The catalyst components indicated by X and/or Y were added immediately before the addition of 5.8 9 85% phosphoric acid. 2.59 hydrazine hydrate was added in all preparations, except that no hydrazine was added in examples 28, 30, 32 and 38; and 1.0 g of hydrazine was added in example 14 • To prepare the catalysts, the following compounds and quantities were used:

Example 40

2- 5% M°12P1As0;5NbQ>25Ag0j05O x<+>75% - Alundum"

This catalyst was prepared in the same manner as described in Example 21, except that 34.25 g of ammonium molybdate, 150 ml of water, 1.28 g of ammonium arsenate, 0.537 g of niobium chloride, 0.134 g of silver acetate, 1.86 g of 85% phosphoric acid and 0.8 g of hydrazine hydrate was used.

Example 4l

25%■ Mo12P1ASo>5Nb0t25Cu0>1Ox<+>75% "Alundum"

This catalyst was prepared in the same way as described in example 24, except that 0.322 g of copper acetate was added in addition to the niobium chloride.

Example 42

25<%>Zn Al_ nQCu M0l„Pn „„Asn ^0<+>75% "Alundum"

0 , 2 0 , 08 0 , 05 12 1 , 32 0 .5 x ,

This catalyst was prepared in the same manner as described in Example 37, except that. 0.96 g of aluminum chloride hydrate and 7.6 g of 85% phosphoric acid were used.

Example 43

25F°-Re0, lA10, 091CU0, 05MO12Pl, 32AS0, 5°x + 75% "Alundum"

This catalyst was prepared in the same manner as described in Example 42, except that 1.1 g of aluminum chloride hydrate and 1.21 g of Re 2 O 3 were used.

Comparative Examples B to D and Examples 4 4 to 67

The results of the experiments using catalysts of formula II in the oxidation of methacrolein to methacrylic acid are shown in Table II. The same definitions as described above,

is used when measuring the carbon atoms in the feed and the products.

In the same way as described above, the catalysts according to the invention can be effectively used in the production of acrylic acid from acrolein.

Examples 68 to 73

Various catalysts of formula III were prepared

as follows:

Example 68

25% AgQ 25Mol2PlAsO 5°x + 75% "Alundum"

A solution was prepared consisting of 105.99 ammonium heptamolybdate, ( NH^ ) ^MoyD^ .4H20 , (0.6 mol Mo), 700 ml of distilled water at 6o°C and 4.0 g of ammonium arsenate, NH^H2AsO^, (0.025 mol As), as a solution in 25 ml of water. A white precipitate was formed which was heated at 100°C for approx. half hour. To this mixture was added 2'.08 g of silver acetate (0.0125 mol Ag), followed by the addition of 5.8 g of 85% phosphoric acid (0.05 mol P). Half an hour later, 2.5 g of hydrazine hydrate were added. The slurry was evaporated to a thick paste, dried overnight in an oven at 110 - 120°C, and ground and sieved to below 80 mesh size. The catalyst was then coated to 25% active level on 3.2 mm "SA 5223" "Alundum" beads. The calcination was the same as in Comparative Example A.

Example example 69

25<%>AU0, 05CdO, 2Mol2Pl, 0AsO, 5Qx<+>75% "Alundum"

This catalyst was prepared in the same way as described

in Example 68, except that 150 ml of water, 34.25 g of ammonium molybdate, 1.28 g of ammonium arsenate, 0.862 g of cadmium acetate, 0.318 g of gold chloride, .1.86 g of 85% phosphoric acid and 0.89 g of hydrazine hydrate. was applied.

Example 70

25% Ruo,2Mol2PlAsO 5Qx + 75% "Alundum"

This catalyst was prepared in the same way as described

in Example 68, except that 500 ml of water, 70.6 g of ammonium molybdate, 2.64 g of ammonium arsenate, 1.74 g of ruthenium chloride, RuCl^I-^O,

(0.006 mol Ru), . 3.84 g of phosphoric acid and 1.6 g of hydrazine hydrate were used.

Examples 71 to 73

Preparation of the catalysts 25% X Y Mo P Ac n

_+ 75% "Alundum" b l2 l 0.5 x

Various catalysts according to the invention were prepared. The catalysts were prepared by the method of Example 68, using 105.9. 9 ammonium molybdate, 700 ral of distilled water of 6o°C and 4.0 g of ammonium arsenate dissolved in 25 ml of water. The catalytic components denoted by X and/or Y were added immediately before the addition of 5.8 g of 85% phosphoric acid and 2.5 g of hydrazine hydrate. To prepare the catalysts, the following compounds and quantities were used:

Comparative Examples B to D and Examples 74 to 80

The results of the experiments using catalysts of formula III in the oxidation of methacrolein to methacrylic acid are shown in Table III. The same definitions as described above were used to measure the carbon atoms in the feed and in the products.

In the same way as described above, the catalysts according to the invention can be effectively used in the production of acrylic acid from acrolein.

Claims (17)

1. Process for the production of acrylic acid and methacrylic acid by oxidation of acrolein, respectively. methacrolein, with molecular • oxygen in the vapor phase at a reaction temperature of 200 - 500°C in the presence of a catalyst, and possibly in the presence of steam, characterized in that a catalyst with the formula is used: where X is a rare earth element or a mixture thereof; Y is at least one element selected from the group consisting of Ag, Tl, Rh, Pd, Ru, Pt, Cd, Al, Au, Cu, alkaline earth metal, Cl and Nrl^; where' a is 0.001 to 10; b is 0 to 10; c is 0.01 to 5; d is 0.01 to 5; x is the number of oxygen atoms required to satisfy the valence states of the other elements present. 2. Method according to claim 1, characterized in that X is cerium, erbium or a mixture of rare earth elements consisting essentially of Ce, La, Nd and Pr.. 3. Method according to claim 1 or 2, characterized in that X is a mixture of rare earth elements, consisting essentially of Ce, La, Nd and Pr. Method according to claim 1, characterized in that X is cerium. 5. Method according to claim 1, characterized in that X is erbium. 6. Method according to claim 1, characterized in that Y is at least one of the metals silver, thallium and copper. 7. Procedure according to claim 1, characterized in that Y is sblv. 8. Procedure according to claim 1, characterized in that Y is thallium. 9. Method according to claim 1, characterized in that Y is copper. 10. Method according to claim 1, characterized in that b is zero. 11. Method according to claim 1, characterized in that a is 0.001 to 3. 12.. Method according to claim 1., characterized in that b is 0.001 to 3. 13. Procedure according to claims 1-12, characterized by the active catalytic, material is coated on an inert carrier. lh. Method according to claims 1-13, characterized in that the catalyst essentially consists of an inert carrier material with a diameter of at least 20 µm and an outer surface and a continuous coating of the active catalyst adhering strongly to the outer surface of the carrier. 15. Method according to claims 1 - 14, characterized in that the active catalyst material constitutes 10 - 100% of its weight. inert. carrier. 16. Method according to claim 13 - 155, characterized in that the carrier is selected from the group consisting of silicon oxide, aluminum oxide, "Alundum", aluminum oxide-silicon oxide, silicon carbide, titanium dioxide and zirconium dioxide. 17. Method according to claims 13-16, characterized in that the particle size of the inert carrier is 0.2 - 2 cm.