Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
  • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
  • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
  • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
  • C07D251/40—Nitrogen atoms
  • C07D251/54—Three nitrogen atoms
  • C07D251/56—Preparation of melamine
  • C07D251/60—Preparation of melamine from urea or from carbon dioxide and ammonia

Definitions

• the present application relates to a process for the production of melamine by catalytic decomposition of urea.
• the process according to the invention is a two-stage process in which catalysts of different acidity are used in each of the two stages.
• melamine resins by reaction with carbonyl-containing compounds.
• the resins are used used as plastics as well as in paints and varnishes.
• the production of melamine by the decomposition of urea is a known reaction which is used in several variants by the chemical industry. A basic distinction is made between the high-pressure and the low-pressure process.
• the high pressure process is carried out at pressures of> approx. 80 bar (abs.) And temperatures> 370 ° C, whereby the melamine synthesis takes place in a non-catalytic manner.
• the low-pressure process which is carried out at pressures of approximately 1 to 10 bar (abs.) And temperatures of 370 to 430 ° C., is of greater importance. It is known that the reaction takes place in two steps. In the first, endothermic step, urea reacts to ammonia and isocyanic acid, which in the second, exothermic step trimerizes to melamine with the release of CO.
• the following equations represent the individual implementations.
• the implementation is carried out in two stages.
• molten urea is decomposed into ammonia and isocyanic acid in a fluidized bed of sand, at 350 ° C. and 3.5 bar (abs.).
• Isocyanic acid is then catalytically converted to melamine at 450 ° C. and atmospheric pressure in a fixed bed reactor.
• the catalyst is generally an aluminum oxide catalyst.
• the DSM Stamicarbon process is a one-step process that is carried out at approx. 7 bar (abs.).
• Aluminum silicates which are used as a fluidized bed, serve as the catalyst.
• Pure ammonia is used as the fluidizing gas, which is recovered via exhaust gas processing.
• the excessive deposition of the condensation products is accompanied by a deactivation of the catalyst, which requires regeneration thereof, for example by thermal treatment and / or treatment with water vapor, air or ammonia, but in extreme cases also necessitates an exchange of the catalyst.
• deactivation often occurs after a very short period of time, so that periodic regeneration is out of the question due to the short time intervals.
• JP-A 08 027 126 claims a ⁇ -Al 2 O 3 catalyst with defined acidity limits for melamine synthesis.
• the object of the present invention is to provide a process by means of which high conversions and melamine yields can be achieved without an early catalyst deactivation due to deposit formation, in particular under the chosen reaction conditions.
• This object is achieved by a process for the catalytic production of melamine by decomposing urea over solid catalysts using a main and post-reactor, characterized in that a catalyst of low Lewis acidity in the main reactor and a catalyst of the same or higher Lewis Acidity is used.
• the present invention is based on the knowledge that the use of a catalyst with a high Lewis acidity causes a high conversion of the urea starting material to melamine and thus leads to high reaction yields, but the formation of deposits quickly occurs on the catalyst used. The desired effect of the high conversion is thus quickly compensated negatively by the deactivation of the catalyst as a result of the formation of deposits.
• a catalyst of low Lewis acidity is used, which results in a comparatively low conversion, but also only a low formation of deposits.
• a catalyst is used which has the same or a higher Lewis acidity.
• the catalyst in the post-reactor preferably has a higher Lewis acidity, which enables a very high conversion. A high total conversion can thus be achieved, with at the same time little deactivation both of the catalyst used in the main reactor and of the catalyst used in the post-reactor.
• the catalyst can in principle be present in all forms known to the person skilled in the art, for example as a fixed bed, fluidized bed, circulating fluidized bed or moving bed.
• the catalyst is preferably used as a fluidized bed.
• the catalyst used in the main reactor preferably contains at least one mineral from the group of aluminum oxides, silicon oxides and aluminum silicates or mixtures of different aluminum oxides, silicon oxides and / or aluminum silicates. It particularly preferably contains at least one mineral from the group consisting of bayerite, boehmite, gibbsite, montmorillonite, bentonite and muscovite, in particular bentonite.
• the catalyst can also consist entirely of the minerals mentioned.
• the minerals mentioned may have been activated in a manner known to the person skilled in the art before use, for example by thermal treatment. Since the acidity of the minerals mentioned generally increases during thermal treatment, this is generally not carried out with the catalysts used in the main reactor.
• the catalysts used in the main reactor preferably have a surface Lewis acidity of 0.3 to 1.8, more preferably 0.5 to 1.5, in particular 0.8 to 1.2 ⁇ mol / g.
• the values given were carried out by acidity measurements in a high-vacuum Fourier transform infrared system (HV-FTIR) at a temperature of 390 ° C. using pyridine as the probe molecule, and the Lewis centers characterized by different IR absorption bands were quantified by integrating the peak areas detected.
• HV-FTIR high-vacuum Fourier transform infrared system
• Typical fluidized bed catalysts have BET surface areas of 50 to 350 m 2 / g, preferably 100 to 250 m Ig. Pore volumes are between 0.1 and 1.0 ml / g. The average particle size of the catalysts is 10 to 500 ⁇ m.
• the process in the presence of the catalysts mentioned is carried out at temperatures of 350 to 450 ° C., preferably 380 to 420 ° C., an absolute pressure of 1 to 15 bar, preferably 1 to 10 bar, in particular 5 to 8 bar, of a residence time over the fluidized bed 1 to 50 s, preferably 2 to 30 s and a catalyst load of 20 to 700 kg urea / t (cat) • h, preferably 50 to 500 kg urea / t (cat) • h.
• the main reactor can usually have a cylindrical or conical shape.
• the main reactor as a fluidized bed reactor is conical. This results in a higher velocity of the incoming gas and thus a more stable swirl behavior.
• the catalyst used in the post-reactor preferably has a volume-normalized surface Lewis acidity which is 1.5 to 6 times, preferably 3 to 5 times higher than the catalyst used in the main reactor under reaction conditions.
• the surface acidity of the catalysts used in the post-reactor is preferably from 2 to 12, more preferably 3 to 10, in particular 3.5 to 6 ⁇ mol / g.
• the values given were carried out by acidity measurements in a high-vacuum Fourier transform infrared system (HV-FTIR) at a temperature of 390 ° C. with pyridine as the probe molecule and the Lewis centers characterized by different IR absorption bands were quantified by integrating the peak areas detected.
• HV-FTIR high-vacuum Fourier transform infrared system
• the catalyst in the post-reactor preferably contains at least one mineral from the group consisting of aluminum oxides, silicon oxides and aluminum silicates or mixtures of aluminum oxides, silicon oxides and / or aluminum silicates.
• the catalysts used in the post-reactor contain 0 to 60% by weight, preferably 5 to 50% by weight, SiO 2 and 100 to 40% by weight, preferably 95 to 50% by weight, Al 2 O 3 .
• Alumosilicate catalysts are preferably used.
• the catalysts have BET surface areas of 150 to 400 m 2 / g, preferably 200 to 350 m 2 / g.
• the measures required to achieve the necessary acidity are known to the person skilled in the art. This can be done by incorporating ions of different valence in a given mineral (e.g. silicon dioxide in aluminum oxide) and / or heat treatment.
• the minerals mentioned are activated by heat treatment before use, at temperatures of 350 to 950 ° C., preferably 450 to 750 ° C.
• the pore volumes of the catalysts are 0.1 to 1.5 ml / g, preferably 0.2 to 0.9 ml / g (N 2 ) or 0.1 to 2.0 ml / g, preferably 0.2 up to 1.0 ml / g (mercury porosometry).
• the pore diameter is 10 to 100 ⁇ , preferably 30 to 90 ⁇ .
• the process according to the invention is carried out in the after-reactor with residence times of 0.1 to 20 s, preferably 0.5 to 10 s, and catalyst loads of 0.05 to 2 g HNCO / g (cat) • h, preferably 0.1 to 1 g HNCO / g (Kat) • h performed.
• the temperature is 350 to 500 ° C., preferably 390 to 450 ° C.
• the pressure is 1 to 15 bar absolute, preferably 1 to 10 bar, in particular 5 to 8 bar absolute.
• the catalyst can be in a suitable form known to those skilled in the art, for example as a fixed bed or fluidized bed. It has proven to be advantageous if the catalyst in the post-reactor is in a form in which only a slight backmixing occurs during the reaction. This is the case, for example, with fixed bed catalysts, so that the use of a fixed bed catalyst in the after-reactor is preferred.
• the fixed bed catalyst is advantageously in the form of a shaped body. Shaped bodies which are continuous for the fine catalyst dust removed from the main reactor, for example hollow strands, monoliths, star strands, tablets or grit, are preferably selected here. Honeycomb bodies or hollow strands, in particular honeycomb bodies, are particularly suitable. Of the moldings mentioned, honeycomb bodies have the best properties with regard to the pressure difference during the passage of the reaction gases.
• Honeycomb bodies are preferably used which are made entirely of ⁇ -
• Alumina consist or consist essentially of ⁇ -alumina.
• Honeycomb bodies which contain 60 to 100% by weight of ⁇ -Al 2 O 3 and 0 to 40% by weight of SiO 2 are preferred.
• the mass which can be formed into honeycomb bodies is mixed dry and mixed with a peptizing agent, preferably nitric acid, with water and then rolled.
• a peptizing agent preferably nitric acid
• Suitable peptizing agents are known to the person skilled in the art.
• organic auxiliaries can also be added, which decompose without residue in the heat. Examples are carbonates and cellulose derivatives. Specific examples include ammonium carbonate, ammonium oxalate and hydroxymethyl cellulose (such as that sold under the name Wa locel ®, Wolff Walsrode).
• the moved mass is then extruded under pressure to the desired honeycomb geometry.
• the moldings are dried and finally calcined, preferably at a temperature ⁇ 600 ° C.
• the process is preferably carried out in such a way that most of the conversion takes place in the main reactor and a smaller part of the conversion (residual conversion) in the post-reactor.
• urea was converted to melamine at a temperature of approx. 400 ° C.
• the three catalysts investigated (calcined silicon-doped aluminum oxide (cat 1), calcined aluminum oxide (cat 2) and non-calcined aluminosilicate of the montmorilonite type (cat 3)) had Lewis acidities under reaction conditions of 4.4 or 3.6 and 3.6, 1, 0 ⁇ mol / g.
• the amount of fluidizing gas was approx. 300 Nm 3 / h.
• Fig. 1 shows, the initial conversion of the most acidic catalyst (Cat 1) is highest at around 90%. However, the catalyst is deactivated after a running time of approx. 250 hours; after 450 hours the conversion is already below 60%. Along with the catalyst deactivation is the build-up of organic coating on the catalyst, which is responsible for the deactivation.
• Figure 3 shows the corresponding test with the least acidic catalyst (Cat 3, Lewis acidity only 1 ⁇ mol / g).
• the catalyst shows a conversion of only about 75%, but runs with constant conversion due to the constant organic coating.
• the catalyst used in the fixed bed post-reactor was 10 ⁇ 20 ⁇ 5 mm hollow strands made of silicon-doped aluminum oxide with the composition 95% Al 2 O 3 and 5% SiO 2 , which after extrusion were calcined at 550 ° C. overnight.
• honeycomb bodies with an edge length of 45 x 45 mm and a length of 320 mm are extruded, the 6 x 6 cells with an internal dimension of 5.7 x 5.7 mm and have a web thickness of 1.8 mm.
• the moldings are dried at room temperature. In the drying cabinet, the honeycombs are dried for 24 hours at 30 ° C, then in 10 ° C steps for 24 hours to 60 ° C. The honeycombs are dried at 60 ° C. for a further 24 hours. Finally, the honeycombs are calcined at 500 ° C for seven hours.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Catalysts (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

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Citations (3)

• 2004
  • 2004-01-16 WO PCT/EP2004/000327 patent/WO2004065371A1/de not_active Ceased
  • 2004-01-16 EP EP04702691A patent/EP1587797B1/de not_active Expired - Lifetime
  • 2004-01-16 AT AT04702691T patent/ATE477247T1/de active
  • 2004-01-16 DE DE502004011507T patent/DE502004011507D1/de not_active Expired - Lifetime
  • 2004-01-16 JP JP2006500588A patent/JP4531744B2/ja not_active Expired - Fee Related
  • 2004-01-16 KR KR1020057012980A patent/KR101102121B1/ko not_active Expired - Fee Related
  • 2004-01-16 US US10/542,306 patent/US7253280B2/en not_active Expired - Fee Related

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