Process for preparing a catalyst system for selective alkylation of toluene with propylene

Abstract

The object of the invention is a catalyst system for selective alkylation of toluene with propylene. The catalyst system contains metallic sodium which has been thermally decomposed from sodium azide (NaN.sub.3) or sodium oxide (Na.sub.2 O) onto the surface of solid K.sub.2 CO.sub.3. The invention further concerns a procedure for preparing this catalyst system and a procedure for selectively alkylating toluene with propylene in the presence of a catalyst system.

Description

BACKGROUND OF THE INVENTION

The invention concerns a catalyst system and procedure for selective alkylation of toluene with propylene.

There are two main methods to industrially produce alkylbenzene. One is Friedel-Crafts-catalyzed alkylation of the ring in aromatic compounds, which has the drawback that it tends to lead to polysubstitution (ring substitution) and, thereby, to a wide product range. The other method is to use base catalysts, such as Li, Na or K metals, in the reaction between aromatic hydrocarbons and olefines. Alkali metals may be used as such, or dispersed on the surface of an inorganic carrier substance. An efficient side chain alkylating catalyst is obtained when metallic sodium is dispersed on the surface of dry potassium carbonate. When a basic alkali metal catalyst is used, alkylation takes place selectively in the side chain of the alkylaromatic and no ring substitution occurs, as is the case with acid Friedel-Crafts catalysts. The drawback is comparatively low selectivity of the alkali metal catalyst to aromatics and its tendency to produce various isomers of alkylbenzene, which have to be separated subsequently. Aliphatic dimers are also produced, although these are easily separated from the alkylbenzenes by distillation.

The selectivity of an alkyl metal catalyst is lowered at the preparation stage by oxygen and water residues in the K.sub.2 CO.sub.3 carrier, whereby oxides and hydroxides are formed from part of the active metal. It is for this reason necessary to dry the carrier well at 120.degree.-150.degree. C. in vacuum for 10-20 hours and to prepare the catalyst in an inert atmosphere or in vacuum.

Martens et al. (Scientific bases for the preparation of heterogeneous catalysts, 4th Internat. Symp., Belgium, 1986, F3.1-3.11, and Preparation and catalytic properties of ionic sodium clusters in zeolites, Nature, 315, (1985), p. 568-470) have suggested that sodium azide (NaN.sub.3) is decomposed at 350.degree.-400.degree. C. to three different modifications: metallic sodium (Na.sub.x.sup.o) crystalline metal clusters (Na.sub.y.sup.o) and ionic clusters (Na.sub.4.sup.3+). When NaN.sub.3 was in this way thermally dispersed on the surface of a zeolite, a basic catalyst was thus obtained which was appropriate for use in isomerizing cis-2-butylene. Of azide and carrier substance either a mechanical mixture was prepared or a methanol suspension, from which the azide was decomposed in a tubular reactor to become sodium on the surface of the carrier.

SUMMARY OF THE INVENTION

The object of the invention is to utilize a decomposition reaction as described for preparing a catalyst for use in the toluene alkylating reaction.

The catalyst system of the invention is thus characterized in that it contains metallic sodium which has been thermally decomposed from a compound containing sodium, on the surface of solid K.sub.2 CO.sub.3.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graphical illustration of decomposition of sodium azide as compared with the NaN.sub.3 /K.sub.2 CO.sub.3 combination in accordance with the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The decomposition of sodium azide and of the NaN.sub.3 /K.sub.2 CO.sub.3 mixture was gravimetrically studied, to begin with. (The results of thermoanalysis are shown in FIG. 1.) The graphs reveal that sodium azide decomposes when pure at 400.degree. C. explosively. Mixing with K.sub.2 CO.sub.3 makes the decomposition more leisurely and causes it to take place at a somewhat higher temperature. The decomposition to nitrogen and metallic sodium proceeds according to equation 1:

2NaN.sub.3 .fwdarw.2Na+3N.sub.2 (1) Since the catalyst can be prepared in the reactor tube in situ, awkward catalyst transfers are avoided and the risk of deactivation of the alkali metal catalyst, sensitive to air and moisture, will be less. It is also an advantage that no readily inflammable alkali metals, oxidizing in air, need be handled.

In the way above described, an alkali metal catalyst was prepared in which NaN.sub.3 was thermally decomposed to lodge on the surface of solid potassium carbonate (K.sub.2 CO.sub.3). Furthermore, an alkali metal catalyst was prepared on which NaO.sub.2 was thermally decomposed to lodge on the surface of solid K.sub.2 CO.sub.3.

The properties of the catalysts thus prepared were tested by side chain alkylating toluene with propylene and comparing the results obtained with corresponding results obtained when using a so-called basic catalyst. In the basic catalyst, metallic sodium had been dispersed on the surface of potassium carbonate at high temperature in a nitrogen atmosphere.

PREPARATION OF THE CATALYSTS

A. Azide Catalysts

Three catalysts were prepared, using different azide contents in the NaN.sub.3 +K.sub.2 CO.sub.3 mixtures. The catalysts ATS 4 and ATS 5 were produced in a tubular reactor.

The NaN.sub.3 /K.sub.2 CO.sub.3 mixture was charged, in the form of a mechanical mixture of a methanolic suspension, into a reactor tube through which an N.sub.2 flow could be conducted or vacuum could be drawn. The reactor was heated in a tube furnace, and the inside temperature of the reactor was measured. Decomposition of NaN.sub.3 was observed by increased gas generation. Decomposition took place, with the different catalysts, in the temperature range from 350.degree. to 420.degree. C.

The catalyst ATS 6 was prepared in a 2 dm.sup.3 charge reactor provided with stirring. In Table 1 is shown a summary of the conditions in which the catalysts were prepared, of the quantities of starting materials, and of the manufacturing procedures.

TABLE 1______________________________________Summary of catalyst preparation Manu- Suspen- NaN.sub.3, De- fact. sion/ NaN.sub.3, K.sub.2 CO.sub.3, % Na, Comp. Pro- Mech.Catal. g g oC % temp., cess mixt.______________________________________ATS 4 10.2 40.8 20.0 8.1 360 Tube Suspen- sionATS 5 14.3 21.5 40.0 19.1 390 Tube Suspen- sionATS 6 68.0 176.0 28.0 12.0 420 Charge Mech. mixt.______________________________________

B. Na.sub.2 O+K.sub.2 CO.sub.3 Catalyst

The catalyst of Na.sub.2 O and K.sub.2 CO.sub.3 was prepared by charging an Na.sub.2 O+K.sub.2C O.sub.3 mixture in nitrogen atmosphere into a 1 dm.sup.3 Parr autoclave. The mixture was heated to 270.degree. C. 6 g Na.sub.2 O and 225 g of K.sub.2 CO.sub.3 were used, making the proportion of Na in the mixture 16%, calculated as pure sodium.

Testing of the catalysts

The efficiency in side chain alkylation of toluene of the catalysts that were prepared was tested in charge tests. A 1 dm.sup.3 Parr autoclave with mixer was used for testing apparatus. The test conditions were selected as follows: for azide catalysts--reaction temperature T=170.degree. C., reaction time t=20 h, catalyst mass about 20.0 g, mole proportion of toluene and propylene about 1; for oxide catalysts--T=175.degree. C., t=23 h, and catalyst 28.5 g, mole proportion 0.7. The products were analyzed by gas chromatography. Results of the test runs in Table A.

The results were compared with the tests carried out under the same conditions with the so-called basic catalyst. In the basic catalyst, metallic sodium has been dispersed onto solid potassium carbonate.

Table A reveals that conversion of the starting materials to products was best in the test made with catalyst ATS 5. The mass proportion of sodium in the catalyst is 15% by weight if complete decomposition of the azide used is assumed. The activities of the catalysts regarding isobutylbenzene are nearly equal with the azide catalysts and the basic catalyst; this shows that azide catalysts are well usable in selectively alkylating toluene. With the azide catalysts the proportion of 4-methyl-1-pentene in the product mix is considerably less than with the basic catalyst, whereas the proportion of other hexenes correspondingly increases.

Thus, the results that have been obtained indicate that by decomposing sodium azide or sodium oxide thermally onto solid potassium carbonate a catalyst is obtained which selectively catalyzes the side chain alkylation of toluene with propylene. The principal product in the reaction is isobutylbenzene. In addition, the product contains n-butylbenzene and, as propylene dimerization products, hexenes, which are various methylpentene isomers and straight chain hexenes.

TABLE A__________________________________________________________________________Product distribution obtained with different catalysts SELECTIVITIES ACTIVITY (g/g cat.) CONVERSION Other Isobutyl- n-butyl- Propylene Toluene 4MIP Hexenes benzene benzeneCATALYST % % % % % % IBB n-BB 4MlP__________________________________________________________________________ATS-4 31.35 17.12 3.25 4.79 73.64 7.26 2.13 0.21 0.09ATS 5 54.24 33.29 1.40 9.88 70.96 6.61 4.41 0.41 0.09ATS-6 38.32 33.07 3.84 7.31 70.75 7.22 3.70 0.38 0.20Basic catalyst 41.32 28.22 5,85 5,60 73.96 6.25 3.67 0.31 0.29Na.sub.2 O/K.sub.2 CO.sub.3 24.86 18.14 4.30 4.07 65.94 6.26 1.58 0.15 0.10__________________________________________________________________________ IBB = Isobutylbenzene nBB = butylbenzene 4MlP = 4methyl-l-pentene

Claims

1. Procedure for preparing a catalyst system for selective alkylation of toluene with propylene, containing metallic sodium which has been thermally decomposed from a compound containing sodium, onto the surface of solid K.sub.2 CO.sub.3,

wherein the compound containing sodium is thermally decomposed onto the surface of the solid K.sub.2 CO.sub.3, and

the compound containing sodium is sodium azide (NaN.sub.3).

2. Procedure for preparing a catalyst system for selective alkylation of toluene with propylene, containing metallic sodium which has been thermally decomposed from a compound containing sodium, onto the surface of solid K.sub.2 CO.sub.3,

wherein the compound containing sodium is thermally decomposed onto the surface of the solid K.sub.2 CO.sub.3, and

the compound containing sodium is sodium oxide (Na.sub.2 O).