Patent Application
20140213823
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Not Applicable
The present invention relates to catalytic amination of alkanolamines or glycols with ammonia to form diamines, polyamines, alkanolamines and piperazine, or their derivatives by employing the catalyst composed of two active elements from the transition metal family, namely nickel and chromium, uniformly combined with a refractory microporous substrate. This process operates at lower temperatures and pressures than have hitherto been used commercially.
A considerable number of methods for production of alkylamine products have been proposed and a number of them have been commercially utilized.
It is believed that two mechanisms are prominent in this process and they are: Reductive Amination and Hetergeneous Catalysis.
Reductive Amination: For Ethylene Diamine formation the previous studies on ammonalysis of various alcohols is useful since alcohols, such as ethanol and butanol are known to go via their corresponding aldehyde to primary, secondary and tertiary amines. Other studies have isolated the intermediate aldehyde, (Pasek et al, 1972) (Baiker and Ridaz 1977). The most direct evidence is by (Bashirov, 1971) who used isotope labeling to verify the mechanism.
Heterogeneous Catalysis: This is the straightforward reaction of —OH and —NH or NH2 to form secondary or cyclic amines.
Reductive amination via catalytic hydrogenation of a mixture of aldehyde or ketone and ammonia leads to a predominance of primary amine when excess ammonia is present. At least five equivalents of ammonia should be used; smaller amounts result in formation of more secondary amine.
Various catalysts are manufactured and developed for amination of amines, some of which are listed below:
U.S. Pat. No. 4,209,424 discloses a catalyst for implementing a process for manufacturing amines from alcohols composed of an active element in the transition metals family uniformly combined with a refractory porous structure with a specific surface of between 10 and 300 m2/g and with a pore diameter less than 5000 A. A stabilizer in the form of a sodium-based compound with a sodium content of 0.15 to 20% by weight relative to the weight of the catalyst, and a promoter in the form of a rhodium-based compound with a maximum rhodium content of 0.1% by weight relative to the weight of the catalyst, may be associated with the active metal. The catalyst and the process are applicable to the ethanolamine-ammonia reaction with a view to producing ethylenediamine, piperazine, and useful byproducts. The amination reaction is carried out at 170° C. and 260° C.
U.S. Pat. No. 4,123,462 discloses nickel-rhenium catalyst and catalytic amination of lower aliphatic alkane derivatives such as alkanemono-ols, alkanediols and alcoholamines utilizing the said nickel-rhenium catalyst. The amination reaction is carried out at 125° C. to 350° C.
U.S. Pat. No. 7,601,875 discloses a process for the preparation of ethyleneamines by reacting monoethanolamine (MEOA) with ammonia in the presence of a catalyst in a reactor and separating the resulting reaction product, which comprises reacting ethylenediamine(EDA) obtained during the separation in a separate reactor in the presence of a catalyst to give diethylenetriamine (DETA), and the resulting reaction product is passed to the separation of the reaction product resulting from reactor. The reaction is carried out at temperature of 170° C. and a pressure of 200 bar.
U.S. Pat. No. 6,534,441 disclosesnickel/rhenium catalyst composition for the reductive amination of lower aliphatic alkane derivatives.
Process for production of ethylenediamine carried out by reacting ammonia with monoethanolamine in the presence of a catalyst at 200 to 500° C. in an atmosphere of an inert gas (e.g. nitrogen) according to demand is disclosed in JP3511666. The catalyst is prepared by heat-treating zeolite (e.g. mordenite) in an aqueous solution of EDTA and has a high activity and a long service life.
U.S. Pat. No. 5,410,086 discloses a method for increasing the weight ratio of diethylenetriamine to piperazine at constant Ethylenediamine conversion and constant space velocity in a process in which ethylenediamine and hydrogen are maintained in the presence of a hydrogenation catalyst, which method comprises increasing the hydrogen concentration in the liquid phase in an amount sufficient to effectuate control of the weight ratio of diethylenetriamine to piperazine in said process and catalyst is selected from nickel (Raney nickel), cobalt or rhodium.
A number of production methods are utilized to produce the diamine and polyamine products and various catalysts are developed for these process. These processes, while generally employed throughout the industry, suffer from serious disadvantages.
The currently used processes for producing the products such as Ethylene Diamine, Piperazine, Amino Ethyl Ethanolamine, Diethylene Triamine, AminoethylPiperazine, HydroxyethylPiperazine are cumbersome and a balance has to be struck between conversion per pass of the reactor, selectivity of the large volume products and operating conditions. Generally if one increases conversion, selectivity decreases and more small market yet high value products are formed.
Further these processes utilized for production of aforesaid products are carried out under extremely high pressures (200 kg/cm2g) and temperatures (200-254° C.), far above the critical pressure and temperatures of the reactants. These processes therefore are operating in the supercritical fluid region for ammonia which normally represents >80% of the volume flow to the reactor. At the same time it should be noted that all of the previous patents studied catalysts in a mixture, in a high pressure autoclave, for a fixed contact time not in a flow thru state of the art reactor.
Therefore, there still exists a need in the art to develop a catalyst which helps in manufacturing high value product with higher selectivity and at the same time the process of amination is carried out at low temperature and pressure.
Therefore, it is an object of the present invention to provide process of amination of alkanolamines or glycols with ammonia to form diamines, polyamines and piperazine or their derivatives.
Another object of this invention is to carry out the amination reaction at a pressure much lower than the critical pressure and temperature of the reactants and initiate the reaction at a temperature below 120C.
Yet another object of the present invention is to provide an amination catalyst to be employed in the process of amination of alkanolamines or glycols.
Another object of the present invention is to provide a process of amination having high yield and selectivity of diamines produced during the reaction and to minimize the production of substituted piperazines.
Therefore, in accordance with the above objectives the present invention provides a process of catalytic amination of alkanolamines or glycols with ammonia to predominantly form alkylenediamines, said process comprising reacting said alkanolamines or glycols with ammonia in the presence of a catalyst comprising of at least two active elements from the transition metals nickel and chromium uniformly allied to a refractory porous substrate with a specific surface area between 117 and 147M2/gm.
In another aspect the present invention provides the catalytic amination of alkanolamines or glycols, specifically monoethanolamine or monoethylene glycol, with ammonia to form Ethylene Diamine (EDA); Piperazine (PIP); DiethyleneTriamine (DETA); Amino Ethyl Piperazine (AEP); Amino Ethyl Ethanolamine (AEEA); Hydroxy Ethyl Piperazine (HEP); TriethyleneTetramine (TETA) and TetraethylenePentamine (TEPA) in a Trickle-Down Reactor.
The present invention describes a process for the preparation of an amine using catalyst composed of at least two active elements from the transition metals family and is uniformly allied to a refractory porous substrate with a specific surface area.
In an embodiment the present invention describes a process for the preparation of an amine by reacting an alkanolamine or a polyol with ammonia in the presence of a catalyst composed of two active metals from the group of transition metals consisting of cobalt, nickel, copper, chromium supported on a microporous refractory substrate with specific surface adequate for this reaction in minutes and pore size capable of handling large molecules, see
The transition metals are forty in number. The preferred active metals are nickel and chromium and the total transition metals content represents 60.0±10% of the total active catalyst weight.
The microporous refractory substrate is selected from the group consisting of diatomaceous earth, graphite, alumina or alumina oxide, silica such as silica oxide, Kieselguhr, Attapulgite, thorium oxide and cerium oxide. A specific diatomaceous earth is preferred.
In a preferred embodiment, the present invention provides the amination catalyst for use in the amination of an alkanolamine or glycol. The catalyst of the present invention comprises Nickel and chromium metals deposited on a diatomaceous earth support. The nickel component is present in an amount of 49±5% wt. and the chromium component is present in an amount of 10±2% wt. The catalyst is activated by heating in a stream of hydrogen at 140°-200° C., at atmospheric pressure, for twelve hours or more.
The process for the preparation of an amine using amination catalyst in a heterogeneous phase for producing diamines, polyamines, alkanolamines and piperazine or their derivatives exhibits high conversion and selectivity. Preferably, the present invention relates to use of the provided catalysts in a process for the preparation of diamines, polyamines, alkanolamines and piperazine or their derivatives from polyols and/or alkanolamines.
In another embodiment the present invention describes a process for the production of ethylene diamine, diethylenetriamine, piperazine, aminoethyl piperazine, aminoethyl ethanolamine, hydroxyethylpiperazine, and heavier amines by reacting monoethanolamine and ammonia. Conversion per reactor pass is 50% or more and selectivity to ethylene diamine can be ≧65%.
In yet another embodiment, the present invention describes catalytic amination of alkanolamines or glycols with ammonia to form diamines, polyamines and piperazine or their derivatives as well as alkanolamines using the aforementioned amination catalyst. The reaction is carried out at low pressure and temperature i.e. below the critical zone.
In another embodiment the amination catalyst of the present invention is useful for production of predominantly monoethanolamine by reacting monoethylene glycol and ammonia at high nitrogen/carbon ratios such as 10:1.
The amination catalyst of the present invention is useful for the production of ethylene diamine, diethylenetriamine, piperazine, aminoethylpiperazine, aminoethyl ethanolamine, hydroxyethylpiperazine, and heavier amines by reacting monoethanolamine and ammonia. Further the amination catalyst is also used for the production of predominantly monoethanolamine from monoethylene glycol and ammonia at high nitrogen/carbon ratios.
The amination catalyst of the present invention affords the conversion of >50% or more of the reactants per reactor pass and selectivity to ethylene diamine is ≧65% with high nitrogen/carbon ratios, then at low nitrogen/carbon mole ratios the conversion per reactor pass is ≧50% and the selectivity of conversion to higher amines exceeds 70%.
In the preferred embodiment the present invention provides a method of producing diamines, triamines, amino alkanolamines, and piperazines using a nickel/chromium catalyst at a temperature of less than 130° C. and a pressure equal to or less than 50 Bar g.
In the most preferred embodiment, the present invention describes a method of producing ethylene diamine, diethylenetriamine, piperazine, aminoethylpiperazine, aminoethyl ethanolamine, hydroxyethylpiperazine, and heavier amines by reacting monoethanolamine and ammonia using a nickel/chromium catalyst at a temperature of less than 130° C. and a pressure equal or less than 50 Bar. The process maintains conversions of greater than 50% and selectivity of greater than 65% EDA.
It is observed that minimizing the temperature and pressure of the reaction also minimizes the more complex reactions as many of the compounds were not detected during the reaction. The reaction products observed in reacting ethylene glycol or monoethanolamine with ammonia over the catalysts of the present invention were: Ammonia (NH3); Ethylene Glycol (EG); Monoethanolamine (MEA); Ethylene Diamine (EDA); Piperazine (PIP); DiethyleneTriamine (DETA); Amino Ethyl Piperazine (AEP); Amino Ethyl Ethanolamine (AEEA); Hydroxy Ethyl Piperazine (HEP); TriethyleneTetramine (TETA) and TetraethylenePentamine (TEPA).
These and other advantages of the invention may become more apparent from the examples set forth herein below. These examples are provided merely as illustrations of the invention and are not intended to be construed as a limitation thereof.
Many permutation and combination of metals and supports were tried before arriving at the selective Ni—Cr Catalyst, some of the major ones are listed below. In all approximately four thousand, hourly tests (e.g.
When aminations were tried using the above range of catalysts, conversions ranged from zero to more than 50% and selectivity of EDA went from zero to 80%. The pressures used were between 71 psig (5 Kg/cm2G) and 710 psig (50 Kg/cm2G) and the reactor inlet temperature could be varied from 70 to 200° C. It was surprisingly found that for the catalyst of the present invention, the pressure range was narrowed to 500 to 710 psig and the temperature range from 70 to 130° C.
The reactor feed composition is extremely important to ensure good conversion and selectivity. It has been found that factors such as Temperature, Pressure, Contact Time, Nitrogen to Carbon Mole Ratio N/C, Water Content of Feed, Hydrogen Content of Feed affects the conversion and product selectivity.
The amination process of the present invention is preferably carried out at temperatures between 90 and 130° C., and the pressures between 500 and 710 psig. Preferably, a contact time of 3 to 7 minutes is sufficient. Contact time and N/C ratio are inter-dependent. For example, for a given mass flow of glycol or alkanolamine at high ammonia/alkyl (N/C) ratios the contact time is less than at low ammonia to alkyl ratios. Water content of 10% or more in the feeds seems to enhance the speed at which ammonia gets into the liquid phase in order to undergo the reaction, hydrogen content of the vapor is about 40-60%. Ammonia to alkyl ratios as high as 20 to 1 have been proposed in some patents but it has been found that ratios in the range of 3:1 to 7:1 are adequate and result in very significant energy savings when the design of full scale plant is studied.
The test reactor as in
