CA1198428A - Catalysis of condensation reactions - Google Patents
Catalysis of condensation reactionsInfo
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- CA1198428A CA1198428A CA000405618A CA405618A CA1198428A CA 1198428 A CA1198428 A CA 1198428A CA 000405618 A CA000405618 A CA 000405618A CA 405618 A CA405618 A CA 405618A CA 1198428 A CA1198428 A CA 1198428A
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Abstract
ABSTRACT
Certain hydrogen phosphate and pyrophosphate compositions are employed as catalysts for organic condensation reactions. Particularly high conversions and selectivities are obtained by the use of synergistic mixtures of in cyclization reactions such as in the conversion of hydroxyethylpiperazine to triethylene-diamine and morpholine to dimethylaminoethylmorpholine.
Certain hydrogen phosphate and pyrophosphate compositions are employed as catalysts for organic condensation reactions. Particularly high conversions and selectivities are obtained by the use of synergistic mixtures of in cyclization reactions such as in the conversion of hydroxyethylpiperazine to triethylene-diamine and morpholine to dimethylaminoethylmorpholine.
Description
~:~9~342~
CATALYSIS OF CONDENSAT10~ REACTIONS
This application is related to copending Canadian Patent Application No.~c~/~2Q~ filed March 31, 1982.
TECHNICAL FIELD OF THE INVENTION
_ _ ~
The present invention relates to organic condensation reactions effected in the presence of novel pyrophosphate and hydrogen phosphate catalysts and is more particularly concerned with the production of amine compounds in enhanced yields.
BACKGROUND OF THE PRIOR ART
Organic synthesis by condensation reactions resulting in the loss of a molecule of water or of ammonia are well known in the art. Certain of such reactions are generally effected in the presence of acidic catalysts. An important area in which such acid catalysis has bee~ employed is in cyclization reactions as in the synthesis of triethylenediamine and its C-substituted homologues. The catalysts more generally used or proposed for use in such cyclization reactions are solid products of the Lewis acid type.
Triethylenediamine, also called diazab-icyclo -[2.2.2]-octane, has been widely employed commercially as a catalyst in organic isocyanate reactions with compounds containing labile hydrogen, as in the production of urethane polymers.
Triethylenediamine (somet.mes hereinafter referred to as TEDA) was initially prepared 34~3 i~ significant ~uantities by methods such as that descri~ed in U.S. Patent No. 2,937,176, by passing aliphatic amines in vapor phase over acidic cracking catalyst, such as silica-alumina dried gel or acid activated clays. Numerous other feed stocks as well as other catalysts are disclosed in subsequent patents for preparation of TEDA as well as C-alkyl derivatives thereo~.
Typical among these are U.S. Patents 2,985,658 and 1~ 3,166,558 employing preferably silica-alumina type catalyst, but listing also other useful solid acid catalysts that can be employed such as alumina in which phosphate or fluoride ion is incorporated (U.S. 2,9~5,658).
Among other catalysts proposed in the patent art for preparation of triethylene diamine and/or C-alkyl homologues thereof, are certain phosphate compounds, particularly aluminum phosphate.
The use of aluminum phosphate as a catalyst in the preparation of heterocyclic compounds from aliphatic amines ~las early disclosed in U.S. Patent 2,467,205, particularly for the preparation of piperazine from ethylenediarnine or from polyethylene polyamine. The use of aluminum phosphate as catalyst in the preparation of triethylenediamine accompanied by piperazine among other by-products is further described in U.S. Patent 3,172,891; while U.S. Patent 3,342,820 describes the use of complex phosphates of alkali metal and trivalent metals in the preparation of C-alkyl TEDA.
U.S. Patent 3,297,701 discloses as catalysts for preparation of TEDA and C-alkyl TEDA, in addition to the preferred aluminum phosphate stated to be superior, other phosphate compounds including calcium and iron phosphates among other listed metal phosphates. In the conversion of N-aminoethylpiperazine to triethylenedi-amine over aluminum phosphate catalyst, at most up to39 mol% triethylenediamine is said to be obtained.
Other o~ the named metal phosphate catalysts in the 1~9~'~2b~
examples of the Ratent obtain yields of less than 10 mol % T~DA.
Acid metal phosphate catalysts, particularly phosphates of boron, aluminum and trivalent iron, have also been proposed for use in intra-molecular cyclic dehydration reactions and other condensation reactions involving amino compounds. Examples of such reactions are found in U.S.
Patent 4,117,227, which discloses conversion of an N-substituted diethanol-amine to the corresponding N-substituted morpholine. U.S. Patent 4,036,881 describes preparation of non-cyclic polyalkylene polyamines by condensation of an alkylene diamine with an ethanolamine. N-hydroxethyl-morpholine is condensed with morpholine in the presence of aluminum phosphate catalyst to form dimorpholino ethane according to U.S. Patent 4,103,087. Similarly, dimorpholinodiethyl ether is obt~ined by condensation of hydroxyethyl morpholine with aminoethyl morpholine over iron, aluminum or boron phosphate in U.S. Patent 4,095,022. Reaction of piperazine with ethanolamine over such acidic metal phosphate produces N-aminoethyl piperazine according to U.S. Patent 4,049,657. U.K. Patent 1,492,359 discloses the preparation of morpholine compounds by reacting an amino-alkoxyalkanol compound over phosphoric acid and similar types of phosphorus-containing substances.
Pyrophosphates of lithium, sodium, strontium and barium have been used as dehydration catalysts; see U.S. Patent 3,957,900. Phosphates and pyrophosphates of strontium and nickel have been used for the dehydrogenation of, for example, n-butene to butadiene under the conditions described in U.S. Patent 3,54].,172.
SUMMARY OF THE INVENTION
In its broadest aspect the present application is concerned with the provision in methods for the synthesis of organic compounds by condensation reactions in the presence of phosphate catalysts, of the improvement which comprises the use as such of catalysts which are selected from the group consisting of the pyrophosphate, monohydrogen A'~ _ 3 _ ~19~2~
phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclusion of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium per se, and mixtures ~hereof.
DETAILED DESCRIPTION OF THE INVENTION
The monohydrogen and dihydrogen phosphate catalysts of the present invention are prepared by reaction of a mono- or diphosphate of an alkali metal or ammonium with a soluble salt of strontium, copper, magnesium, calcium, barium, æinc, aluminum, lanthanum, cobalt, nickel, cerium or neodymium at ambient temperatures. The highest purity and best yields of the present invention are obtained when using the soluble metal salts of a strong acid such as the metal nitrates, in substantially stoichiometric proportion to the phosphate. In aqueous media under these conditions, t'ne reaction mixture is at a pH of about 3.5 to 6.5. In general, to obtain a precipitate of desired high content of the metal monohydrogen or dihydrogen phosphate, the ratio of phosphate to metal salt in the reaction mixture should be such as to have a pH of 5 + 3, or the mixture should be adjusted to that pH range.
The pyrophosphate form of the catalysts of the present invention are prepared by heat treating the metal monohydrogen or dihydrogen phosphate product at temperatures above about 300C up to 750C in the presence of a mixture of steam and air, preferably at least about 20% by ~olume of steam.
For use as a catalyst, the metal pyro-, monohydrogen or dihydrogen phosphate product may be employed in the form of irregular particles of the desired size range prepared by breaking up the washed and dried filter cake or in the form of regular shaped pellets obtained by known methods of casting or extruding or the product -,~
_~ ~ - 4 -~3L9~
may be deposited or otherwise impreynated into the pores of a microporous substrate such as alumina, silica, silica-alumina, and the like. In using the catalyst of the present invention to catalyze organic condensation reactions, substan~ially the same conditions may be employed as when using the known catalysts for the particular synthesis. For optimum results, however, some adjustment in temperature, diluent and/or space rate may be found beneficial.
Some specific examples of the type of organic compounds selectively obtained by the method of this invention include TEDA, the aliphatic a]kylamines such as methylamine, methylethylamine, dimethylethylamine, morpholine, and dimethylaminoethylmorpholine. In the production of these compounds, the temperature is in the range of about 285 to 420C, the pressure is in the range of about 0.1 to 1.5 atmospheres, and the liguid hourly space velocity (LHSV) of the organic feed stock per volume of catalyst is in the range of about 0.05 to 1.5. Preferabl~ depending on the particular reaction, the temperature is in the range of about 300 to 400C, the pressure is in the range o about 0.3 to 1.O atmospheres and the LHSV is in the range of about 0.1 to ~.3 to obtain the highest yields and most econom-ical process. The operable ratio of the organic feedsto water diluent i5 about 10 to 90% on a weight basis and preferably, 20 to 80% by weight. The optimum yield of these compounds is likely to be obtained using the highest temperature in the preferred range at the lowest LHSV.
In the preparation of TEDA, the preferred catalyst is selected from the group consisting of monohydrogen phosphate of calcium, magnesium, zinc, mixtures of strontium and barium in the ratio of Sr to Ba of about 1 to 5 to 5 to 1 and mixtures of lanthanum and strontium in the ratio of La to Sr of about 15 to 1 to 15. The organic feed stock used in this reaction to produce ~842~
TEDA is a substituted piperazine compound selected from the group consisting of hydroxyethylpiperazine and aminoethylpiperazine. The catalysts of this invention are relatively unef~ected by the purity of the feed stock. For example, high conversion and good yields can be obtained from crude hydroxyethylpiperazine which contains minor quantities of piperazine and bis hydroxy-ethylpiperazine.
In the preparation of dimethylaminoethylmorpholine (DMAEM), the preferred catalys~ is a mixture of strontium and nickel monohydrogen phosphate in the ratio of Sr to Ni of about 1 to 5 to 5 to 1. The feed stock is morpholine and dimethylethanolamine in the ~olar ratio in the range of about 1 to 3 and 3 to 1. Preferably, the reaction takes place in the presence of hydrog n in the molar ratio of hydrogen to organic feed of about 1 to 1 to 20 to 1 and an inert gas such as nitrogen, argon or helium in the molar ratio of inert gas to organic feed of about 1 to 1 to 20 to 1.
In the preparation of morpholine compounds, e.g.
morpholine and alkyl morpholine, wherein the alkyl group has from 1 to ~ carbon atoms, diglycolamine compounds, e.g. diglycolamine and alkyl diglycolamines, wherein the alkyl group has from 1 to 6 carbon atoms are preferably carried out in the presence of strontium monohydrogen phosphate at about 300 to 370C with the other conditions remaining the same as that discussed above. This reaction also preferably takes place in the presence of the inert gas in ratios of 2 to 1 to 10 to 1 inert gas to liquid organic feed stock.
The methods and catalysts of this invention are also capable of reacting an alcohol and a nitrogen-containing compound selected from the group consisting of ammonia, aliphatic primary and secondary amines, and aromatic primary and secondary amines to selectively convert this compound to the corresponding symmetrical or unsymmetrical higher molecular weight amine with little, if any, conversion to the corresponding by-products of thermodynamic amine equilibration. The amines and alcohol ln the feed stock each contain 1 to 20 carbons per molecule. Preferably, the catalyst is lanthanum or coppex monohydrogen phosphate and the molar ratio of alcohol to nitrogen-containing compound ranges from about 1 to 6 to 6 to 1.
CATALYST PREPARATION
Example 1 -200 grams of strontium nitrate [Sr(N03)2] was dissolved in distilled water and brought to a total volume of 800 cc with distilled water. To this solution there was added 10 cc of 85% phosphoric acid followed by 34.5 cc of 50% sodium hydroxide added rapidly with vigorous stirring. The resultant fine white precipitate was stixred for 10 minutes, vacuum-filtered and water-washed. The obtained filter cake was air dried in a static oven at approximately 110~C and extruded into 1/8 inch pellets for evaluation.
The obtained product had a surface area of 10-15 m2/g. By X-ray diffraction the principal component was identified as ~ -Sr~P04 with minor quantities of Sr5(0H) (P04)3 and unreacted Sr(NO3)2. Infrared spectroscopy showed a spectrum consistent with SrHP04. (Ref:
Richard A. Nygurst and Ronald O. Kagel, "Infrared spectra of Inor~anic Compounds", page 163, 1971).
Example 2 195 grams of barium nitrate --Ba(NO3)2-- and 53 grams of strontium nitrate --Sr(NO3)2-- were dissolved in distilled water and diluted to 500 cc. 132 grams o dibasic ammonium phosphate --(N~4)2HPO4-- were dissolved in distilled water and diluted to 500 cc with heat.
The three salt solutions were then combined with heat and stirred for about 10 minutes. The combined solution 119842~3 was vacuum filtered and the resulting precipitate was washed with distilled water and air dried overnight in a static oven at approximately 110C. The filter cake was broken up into small (1/8 to 1/4 inch) irregular granules for evaluation. The resulting product had a surface pH of 4-5 as determined by acid base indicators and the ratio of strontium to barium in the product was found to be 1 to 3.5.
Example 3 The procedure for preparing the Example 2 was carried out except that 130 grams of Ba(N03)2 and 106 grams of Sr(N03)2 were dissolved in distilled water in place of the 195 and 53 grams respectively. The product had a surface pH of 4-5 and a Sr/Ba ratio of 2/1 mol/mol.
The resulting catalyst was in the form of a fine powder and was deposited on an inert, low surface area Alundum silica-alumina core using a powder-coating step. The step comprised placing the amount of catalyst to be coated into a jar with the Alundum spheres and rotating on a jar-mill for several days to cause the catalyst powder to adhere to the spheres. The resulting coated spheres contained 25% of the active catalyst and 75%
-- inert.
Example 4 212 grams of Sr(N03)2 were dissolved in distilled - water and diluted to 500 cc. 115 grams of ammonium dihydrogen phosphate --NH4H2P04-- were dissolved in distilled water and diluted to 500 cc. The remaining steps of the catalyst procedure of Example 2 were carried out. The resulting catalyst was believed to contain less than 5% strontium dihydrogen phosphate --Sr(H2P04)2-- with the balance being SrHP04. The surface pH of this catalyst mixture was 4-4.6 in compar-ison to substantially pure strontium monohydrogen phosphate which has a surface pH of 4.8-5.4. Sub-stantially pure strontium dihydrogen phosphate was found to have a surface pH of 0.2-1.2; see Example 21.
The product of this example was deposited on the S silica-alumina spheres in the same manner as set forth under Example 3.
Example 5 The same procedure for preparing the catalyst of Example 1 was carried out except that 236 grams of calcium nitrate --Ca(NO3)2.4H2O-- and 115 grams of NH4H2P04 were combined. The resulting dried catalyst particles were coated on the silica-alumina spheres in the same manner as that of Example 3. The analysis of the catalyst formed by this procedure indicated that it consisted essentially of calcium monodihydrogen phosphate with a Ca/P ratio of 1.009 and a surface pH of 4-6. In contrast, substantially pure calcium monohydrogen phosphate had a surface pH of 5-5.5; see Example 16 below. The presence of a very small amount of calcium dihydrogen phosphate may account for the difference in the surface pH value of this catalyst.
Example 6 The catalyst preparation procedure of Example 2 was repeated except that 212 grams of Sr(NO3)2 were dissolved in place of the mixed barium and strontium nitrate salts and the resulting strontium monohydrogen phosphate catalyst had a surface pH of 4.8-5.2.
Examples 7-15 The following salts were combined and catalysts were prepared in the manner set forth under Example 2:
1~ 984~ZB
CatalystSurface Example Salt _o utions ~ormulation pH _ (~ (b) 7 168g. Nd(N03)3.5H20 80g- (NH4)2 4 2 4 3 8 217g. Ce(N03)3.6H20 ggg- (NH4)2 4 2 4 3 0.2-1.2 9 415g. ~a(N03)3-5H20 198g- (NH4)2HP4 La2(HP4)3 0.2-1.8 202g. Sr(N03)2+ 132g- (NH4)2HP04 SrHP04/LaHP0 4-5 20 grams of (Sr/La=14.9/~) La(N03)3.5H20 10 11 291g. Co(N03)2.6H20 132g. (NH4~2 4 4 4.6-4.8 12 291g. Ni(N03)2.6H~0 132g- (NH4)2HP 4 4 6.2-6.8 13 242g. CuC12.2.5H20 132g- (NH4)2 4 4 14 297g. Zn(N03)2.6H20 132g- (NH4)2 4 4 6.2-6.5 125g. Al(N03)3.9H20 66g. (NH4)2H 4 2 4 3 2 *Colored product, pH N.A.
Example 16 160 grams of Ca(NO3)4 were dissolved in distilled water and diluted to 800 cc. 20 cc. of phosphoric acid ~88% by wt. in water) were added with agitation.
34.5 cc-. of sodium hydroxide solution (50% by wt. NaOH
in water) were added to precipitate the CaHPO4 which was filtered, washed, dried and granulated as in Example 2.
The resulting product had a surface-pH of 5-5.5.
Controls 1-3 The following salts were also combined in the manner of the Example 1 preparation.
~ 91~42~3 Catalyst Con~rol Salt Solutions Formulation , .
~a) (b) 1 261g. ~a(N03)2 230g. NH4HS04 BaS04
CATALYSIS OF CONDENSAT10~ REACTIONS
This application is related to copending Canadian Patent Application No.~c~/~2Q~ filed March 31, 1982.
TECHNICAL FIELD OF THE INVENTION
_ _ ~
The present invention relates to organic condensation reactions effected in the presence of novel pyrophosphate and hydrogen phosphate catalysts and is more particularly concerned with the production of amine compounds in enhanced yields.
BACKGROUND OF THE PRIOR ART
Organic synthesis by condensation reactions resulting in the loss of a molecule of water or of ammonia are well known in the art. Certain of such reactions are generally effected in the presence of acidic catalysts. An important area in which such acid catalysis has bee~ employed is in cyclization reactions as in the synthesis of triethylenediamine and its C-substituted homologues. The catalysts more generally used or proposed for use in such cyclization reactions are solid products of the Lewis acid type.
Triethylenediamine, also called diazab-icyclo -[2.2.2]-octane, has been widely employed commercially as a catalyst in organic isocyanate reactions with compounds containing labile hydrogen, as in the production of urethane polymers.
Triethylenediamine (somet.mes hereinafter referred to as TEDA) was initially prepared 34~3 i~ significant ~uantities by methods such as that descri~ed in U.S. Patent No. 2,937,176, by passing aliphatic amines in vapor phase over acidic cracking catalyst, such as silica-alumina dried gel or acid activated clays. Numerous other feed stocks as well as other catalysts are disclosed in subsequent patents for preparation of TEDA as well as C-alkyl derivatives thereo~.
Typical among these are U.S. Patents 2,985,658 and 1~ 3,166,558 employing preferably silica-alumina type catalyst, but listing also other useful solid acid catalysts that can be employed such as alumina in which phosphate or fluoride ion is incorporated (U.S. 2,9~5,658).
Among other catalysts proposed in the patent art for preparation of triethylene diamine and/or C-alkyl homologues thereof, are certain phosphate compounds, particularly aluminum phosphate.
The use of aluminum phosphate as a catalyst in the preparation of heterocyclic compounds from aliphatic amines ~las early disclosed in U.S. Patent 2,467,205, particularly for the preparation of piperazine from ethylenediarnine or from polyethylene polyamine. The use of aluminum phosphate as catalyst in the preparation of triethylenediamine accompanied by piperazine among other by-products is further described in U.S. Patent 3,172,891; while U.S. Patent 3,342,820 describes the use of complex phosphates of alkali metal and trivalent metals in the preparation of C-alkyl TEDA.
U.S. Patent 3,297,701 discloses as catalysts for preparation of TEDA and C-alkyl TEDA, in addition to the preferred aluminum phosphate stated to be superior, other phosphate compounds including calcium and iron phosphates among other listed metal phosphates. In the conversion of N-aminoethylpiperazine to triethylenedi-amine over aluminum phosphate catalyst, at most up to39 mol% triethylenediamine is said to be obtained.
Other o~ the named metal phosphate catalysts in the 1~9~'~2b~
examples of the Ratent obtain yields of less than 10 mol % T~DA.
Acid metal phosphate catalysts, particularly phosphates of boron, aluminum and trivalent iron, have also been proposed for use in intra-molecular cyclic dehydration reactions and other condensation reactions involving amino compounds. Examples of such reactions are found in U.S.
Patent 4,117,227, which discloses conversion of an N-substituted diethanol-amine to the corresponding N-substituted morpholine. U.S. Patent 4,036,881 describes preparation of non-cyclic polyalkylene polyamines by condensation of an alkylene diamine with an ethanolamine. N-hydroxethyl-morpholine is condensed with morpholine in the presence of aluminum phosphate catalyst to form dimorpholino ethane according to U.S. Patent 4,103,087. Similarly, dimorpholinodiethyl ether is obt~ined by condensation of hydroxyethyl morpholine with aminoethyl morpholine over iron, aluminum or boron phosphate in U.S. Patent 4,095,022. Reaction of piperazine with ethanolamine over such acidic metal phosphate produces N-aminoethyl piperazine according to U.S. Patent 4,049,657. U.K. Patent 1,492,359 discloses the preparation of morpholine compounds by reacting an amino-alkoxyalkanol compound over phosphoric acid and similar types of phosphorus-containing substances.
Pyrophosphates of lithium, sodium, strontium and barium have been used as dehydration catalysts; see U.S. Patent 3,957,900. Phosphates and pyrophosphates of strontium and nickel have been used for the dehydrogenation of, for example, n-butene to butadiene under the conditions described in U.S. Patent 3,54].,172.
SUMMARY OF THE INVENTION
In its broadest aspect the present application is concerned with the provision in methods for the synthesis of organic compounds by condensation reactions in the presence of phosphate catalysts, of the improvement which comprises the use as such of catalysts which are selected from the group consisting of the pyrophosphate, monohydrogen A'~ _ 3 _ ~19~2~
phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclusion of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium per se, and mixtures ~hereof.
DETAILED DESCRIPTION OF THE INVENTION
The monohydrogen and dihydrogen phosphate catalysts of the present invention are prepared by reaction of a mono- or diphosphate of an alkali metal or ammonium with a soluble salt of strontium, copper, magnesium, calcium, barium, æinc, aluminum, lanthanum, cobalt, nickel, cerium or neodymium at ambient temperatures. The highest purity and best yields of the present invention are obtained when using the soluble metal salts of a strong acid such as the metal nitrates, in substantially stoichiometric proportion to the phosphate. In aqueous media under these conditions, t'ne reaction mixture is at a pH of about 3.5 to 6.5. In general, to obtain a precipitate of desired high content of the metal monohydrogen or dihydrogen phosphate, the ratio of phosphate to metal salt in the reaction mixture should be such as to have a pH of 5 + 3, or the mixture should be adjusted to that pH range.
The pyrophosphate form of the catalysts of the present invention are prepared by heat treating the metal monohydrogen or dihydrogen phosphate product at temperatures above about 300C up to 750C in the presence of a mixture of steam and air, preferably at least about 20% by ~olume of steam.
For use as a catalyst, the metal pyro-, monohydrogen or dihydrogen phosphate product may be employed in the form of irregular particles of the desired size range prepared by breaking up the washed and dried filter cake or in the form of regular shaped pellets obtained by known methods of casting or extruding or the product -,~
_~ ~ - 4 -~3L9~
may be deposited or otherwise impreynated into the pores of a microporous substrate such as alumina, silica, silica-alumina, and the like. In using the catalyst of the present invention to catalyze organic condensation reactions, substan~ially the same conditions may be employed as when using the known catalysts for the particular synthesis. For optimum results, however, some adjustment in temperature, diluent and/or space rate may be found beneficial.
Some specific examples of the type of organic compounds selectively obtained by the method of this invention include TEDA, the aliphatic a]kylamines such as methylamine, methylethylamine, dimethylethylamine, morpholine, and dimethylaminoethylmorpholine. In the production of these compounds, the temperature is in the range of about 285 to 420C, the pressure is in the range of about 0.1 to 1.5 atmospheres, and the liguid hourly space velocity (LHSV) of the organic feed stock per volume of catalyst is in the range of about 0.05 to 1.5. Preferabl~ depending on the particular reaction, the temperature is in the range of about 300 to 400C, the pressure is in the range o about 0.3 to 1.O atmospheres and the LHSV is in the range of about 0.1 to ~.3 to obtain the highest yields and most econom-ical process. The operable ratio of the organic feedsto water diluent i5 about 10 to 90% on a weight basis and preferably, 20 to 80% by weight. The optimum yield of these compounds is likely to be obtained using the highest temperature in the preferred range at the lowest LHSV.
In the preparation of TEDA, the preferred catalyst is selected from the group consisting of monohydrogen phosphate of calcium, magnesium, zinc, mixtures of strontium and barium in the ratio of Sr to Ba of about 1 to 5 to 5 to 1 and mixtures of lanthanum and strontium in the ratio of La to Sr of about 15 to 1 to 15. The organic feed stock used in this reaction to produce ~842~
TEDA is a substituted piperazine compound selected from the group consisting of hydroxyethylpiperazine and aminoethylpiperazine. The catalysts of this invention are relatively unef~ected by the purity of the feed stock. For example, high conversion and good yields can be obtained from crude hydroxyethylpiperazine which contains minor quantities of piperazine and bis hydroxy-ethylpiperazine.
In the preparation of dimethylaminoethylmorpholine (DMAEM), the preferred catalys~ is a mixture of strontium and nickel monohydrogen phosphate in the ratio of Sr to Ni of about 1 to 5 to 5 to 1. The feed stock is morpholine and dimethylethanolamine in the ~olar ratio in the range of about 1 to 3 and 3 to 1. Preferably, the reaction takes place in the presence of hydrog n in the molar ratio of hydrogen to organic feed of about 1 to 1 to 20 to 1 and an inert gas such as nitrogen, argon or helium in the molar ratio of inert gas to organic feed of about 1 to 1 to 20 to 1.
In the preparation of morpholine compounds, e.g.
morpholine and alkyl morpholine, wherein the alkyl group has from 1 to ~ carbon atoms, diglycolamine compounds, e.g. diglycolamine and alkyl diglycolamines, wherein the alkyl group has from 1 to 6 carbon atoms are preferably carried out in the presence of strontium monohydrogen phosphate at about 300 to 370C with the other conditions remaining the same as that discussed above. This reaction also preferably takes place in the presence of the inert gas in ratios of 2 to 1 to 10 to 1 inert gas to liquid organic feed stock.
The methods and catalysts of this invention are also capable of reacting an alcohol and a nitrogen-containing compound selected from the group consisting of ammonia, aliphatic primary and secondary amines, and aromatic primary and secondary amines to selectively convert this compound to the corresponding symmetrical or unsymmetrical higher molecular weight amine with little, if any, conversion to the corresponding by-products of thermodynamic amine equilibration. The amines and alcohol ln the feed stock each contain 1 to 20 carbons per molecule. Preferably, the catalyst is lanthanum or coppex monohydrogen phosphate and the molar ratio of alcohol to nitrogen-containing compound ranges from about 1 to 6 to 6 to 1.
CATALYST PREPARATION
Example 1 -200 grams of strontium nitrate [Sr(N03)2] was dissolved in distilled water and brought to a total volume of 800 cc with distilled water. To this solution there was added 10 cc of 85% phosphoric acid followed by 34.5 cc of 50% sodium hydroxide added rapidly with vigorous stirring. The resultant fine white precipitate was stixred for 10 minutes, vacuum-filtered and water-washed. The obtained filter cake was air dried in a static oven at approximately 110~C and extruded into 1/8 inch pellets for evaluation.
The obtained product had a surface area of 10-15 m2/g. By X-ray diffraction the principal component was identified as ~ -Sr~P04 with minor quantities of Sr5(0H) (P04)3 and unreacted Sr(NO3)2. Infrared spectroscopy showed a spectrum consistent with SrHP04. (Ref:
Richard A. Nygurst and Ronald O. Kagel, "Infrared spectra of Inor~anic Compounds", page 163, 1971).
Example 2 195 grams of barium nitrate --Ba(NO3)2-- and 53 grams of strontium nitrate --Sr(NO3)2-- were dissolved in distilled water and diluted to 500 cc. 132 grams o dibasic ammonium phosphate --(N~4)2HPO4-- were dissolved in distilled water and diluted to 500 cc with heat.
The three salt solutions were then combined with heat and stirred for about 10 minutes. The combined solution 119842~3 was vacuum filtered and the resulting precipitate was washed with distilled water and air dried overnight in a static oven at approximately 110C. The filter cake was broken up into small (1/8 to 1/4 inch) irregular granules for evaluation. The resulting product had a surface pH of 4-5 as determined by acid base indicators and the ratio of strontium to barium in the product was found to be 1 to 3.5.
Example 3 The procedure for preparing the Example 2 was carried out except that 130 grams of Ba(N03)2 and 106 grams of Sr(N03)2 were dissolved in distilled water in place of the 195 and 53 grams respectively. The product had a surface pH of 4-5 and a Sr/Ba ratio of 2/1 mol/mol.
The resulting catalyst was in the form of a fine powder and was deposited on an inert, low surface area Alundum silica-alumina core using a powder-coating step. The step comprised placing the amount of catalyst to be coated into a jar with the Alundum spheres and rotating on a jar-mill for several days to cause the catalyst powder to adhere to the spheres. The resulting coated spheres contained 25% of the active catalyst and 75%
-- inert.
Example 4 212 grams of Sr(N03)2 were dissolved in distilled - water and diluted to 500 cc. 115 grams of ammonium dihydrogen phosphate --NH4H2P04-- were dissolved in distilled water and diluted to 500 cc. The remaining steps of the catalyst procedure of Example 2 were carried out. The resulting catalyst was believed to contain less than 5% strontium dihydrogen phosphate --Sr(H2P04)2-- with the balance being SrHP04. The surface pH of this catalyst mixture was 4-4.6 in compar-ison to substantially pure strontium monohydrogen phosphate which has a surface pH of 4.8-5.4. Sub-stantially pure strontium dihydrogen phosphate was found to have a surface pH of 0.2-1.2; see Example 21.
The product of this example was deposited on the S silica-alumina spheres in the same manner as set forth under Example 3.
Example 5 The same procedure for preparing the catalyst of Example 1 was carried out except that 236 grams of calcium nitrate --Ca(NO3)2.4H2O-- and 115 grams of NH4H2P04 were combined. The resulting dried catalyst particles were coated on the silica-alumina spheres in the same manner as that of Example 3. The analysis of the catalyst formed by this procedure indicated that it consisted essentially of calcium monodihydrogen phosphate with a Ca/P ratio of 1.009 and a surface pH of 4-6. In contrast, substantially pure calcium monohydrogen phosphate had a surface pH of 5-5.5; see Example 16 below. The presence of a very small amount of calcium dihydrogen phosphate may account for the difference in the surface pH value of this catalyst.
Example 6 The catalyst preparation procedure of Example 2 was repeated except that 212 grams of Sr(NO3)2 were dissolved in place of the mixed barium and strontium nitrate salts and the resulting strontium monohydrogen phosphate catalyst had a surface pH of 4.8-5.2.
Examples 7-15 The following salts were combined and catalysts were prepared in the manner set forth under Example 2:
1~ 984~ZB
CatalystSurface Example Salt _o utions ~ormulation pH _ (~ (b) 7 168g. Nd(N03)3.5H20 80g- (NH4)2 4 2 4 3 8 217g. Ce(N03)3.6H20 ggg- (NH4)2 4 2 4 3 0.2-1.2 9 415g. ~a(N03)3-5H20 198g- (NH4)2HP4 La2(HP4)3 0.2-1.8 202g. Sr(N03)2+ 132g- (NH4)2HP04 SrHP04/LaHP0 4-5 20 grams of (Sr/La=14.9/~) La(N03)3.5H20 10 11 291g. Co(N03)2.6H20 132g. (NH4~2 4 4 4.6-4.8 12 291g. Ni(N03)2.6H~0 132g- (NH4)2HP 4 4 6.2-6.8 13 242g. CuC12.2.5H20 132g- (NH4)2 4 4 14 297g. Zn(N03)2.6H20 132g- (NH4)2 4 4 6.2-6.5 125g. Al(N03)3.9H20 66g. (NH4)2H 4 2 4 3 2 *Colored product, pH N.A.
Example 16 160 grams of Ca(NO3)4 were dissolved in distilled water and diluted to 800 cc. 20 cc. of phosphoric acid ~88% by wt. in water) were added with agitation.
34.5 cc-. of sodium hydroxide solution (50% by wt. NaOH
in water) were added to precipitate the CaHPO4 which was filtered, washed, dried and granulated as in Example 2.
The resulting product had a surface-pH of 5-5.5.
Controls 1-3 The following salts were also combined in the manner of the Example 1 preparation.
~ 91~42~3 Catalyst Con~rol Salt Solutions Formulation , .
~a) (b) 1 261g. ~a(N03)2 230g. NH4HS04 BaS04
2 75g. CsCl 40g. (NH4)2HP04 CsHP04-~
3 106g. Sr(N03)2 40g. 50% NaOH+ SrHAsO4 80g- (NH4)2H2A54 *Did not form a precipitate.
Control 4 200 grams of Sr(NO3~2 were dissolved in distilled water and diluted to 400 cc. 92 grams of H2SO4 were diluted in 200 cc. of distilled H20 75 grams of 50 wt. % NaOH solution were diluted to 200 cc. with distilled water. The H2SO~ and NaOH solutions were mixed together slowly. ~he Sr(N03)2 solution was stirred into the solution containing H2SO4 and NaOH. The solution was stirred for 10 minutes and the precipitate was filtered, washed and dried. The surface pH of the resulting catalyst was less than 3 which was believed to be substantially all SrSO4.
Example 17 71 grams of Na2HP04 were dissolved in 500 cc. of distilled water. 101.7 grams of MgC12.6H20 were dis-solved in 500 cc. of distilled H2O. Both solutions were mixed together and the precipitate was filtered, washed and dried. The surface pH of the MgHPO4 product was 7-8.
Example 18 71 grams of Na2HP04 and 130.7 grams of Ba(NO3)2 were each separately dissolved in 500 cc. of distilled H2O The 2 solutions were mixed and the precipitate was filtered, washed and dried. The resulting BaHP04 had a surface pH of 8-9.
2~
Each of the products resulting from the procedures of Examples 17 and 18 above were coated on the silica-alumina spheres in the same manner as indicated in Example 3.
Example 19 The SrHP04 catalyst of Example 6 was heat treated for 2 hours in the presence of a mixture 20% by volume steam and the balance air at 350C. The resulting strontium pyrophosphate (Sr2P2O7) had a crushing strength of 0.47 kg./mm of length and a packed bulk density of 1.01 kg./l.
ExamPle 20 The ZnHP04 catalyst product of Example 14 above was coated on the silica-alumina spheres in the manner set forth in Example 3.
Example 21 132.5 grams of strontium hydroxide octahydrate --Sr(OH)2.8H2O-- were dissolved in a solution of 750 cc. of 85% phosphoric acid and 1500 cc. of distilled water. The resulting solution was slowly evaporated to a total volume of about 900 cc. with the temperature being maintained at 25 to 30~C. The solution was cooled to 5C overnight and a whi-te precipitate was recovered by vacuum filtration. The resulting Sr(H2PO4)2 precipitate was washed with 5-300 cc. portions of anhydrous ethanol and with 2-200 cc. portions of anhy-drous ether. The product was dried at room temperature under vacuum for 6 hours. An elemental analysis of the product showed a P/Sr mol ratio of 2.04 and the surface pH was found to be 0.2-1.2. The fine powder was pressed into tablets the size of a typical"Aspirin" (registered trade mark) tablet and crushed to granules 1~8 to 1/4 inch in size.
34Z~
Example 2_ The fine powder of the catalyst prepared in accor-dance with Example 21 was deposited on silica-alumina spheres in the manner set forth in Example 3.
Example 23 2000 grams of Sr~NO3)2 were dissolved in 2000 cc -, of deionized water and the solution diluted to 4000 cc with deionized water after dissolution of the Sr(N03)2 was complete.
In another container, 1342.3 grams of Na2HP04 were dissolved in 2000 cc of deionized water. After solution of the na2HP04 was complete, the solution was diluted to 4000 cc with deionized water. The pH of this solution was approximately 8.~3.
Precipitation of SrHP04 was effected by slowly adding the Na2HP04 solution to the Sr(NO3)2 solution with rapid stirring. The white SrHP04 precipitated rapidly from solution forming a rather thick slurry.
This slurry was mixed for one hour, after which time the pH ~as measured to be about six.
The solid SrHP04 was recovered by filterir.g on an eight frame filter press using cloth filters. It was washed with deionized water. After filtering and washing, the solid was dried in a circulating hot air oven at 250F for four hours. The yield of SrHPO4 was 1680 grams. The solid was wetted and formed into pellets by extrusion through a 3.1 mm die plate and cutting the extrudates to about 1/4 inch in length.
After drying the extrudate at 250F for four hours in a circulating hot air oven, they were heat treated at 662F for two hours in a 20% steam, 80% air atmosphere.
Example 24 106 grams o~ Sr(N03)2 and 145 grams of Ni (N03)2 6H2O were dissolved in distilled water and diluted to ~9~342~3 500 cc. 132 grams of (NH4)2HP04 were dissolved in distilled water and diluted to 50~ cc. the remaini~g steps of Example 1 were carried out to yield a ~Sr-Ni)HPO4 catalyst having a surface pH of 5.4-7Ø
USE OF CATAL~STS
Examples 25-62 Each o~ the prcducts prepared in accordance with Examples 1 through 22 and Controls 1 and 3-5 above were evaluated for catalytic performance for the preparation of TEDA with either a feed mixture containing hydroxy-ethylpiperazine (HEP) or N-aminoethylpiperazine (AEP) in accordance with the following test procedure:
(a) 20 cc (approximately 6.2g.) of the catalyst was loaded into a 3/4 " diameter stainless steel reactor.
(b) The reactor was placed in a conventional tube furnace such that the catalyst bed was near the furnace center and therefore could be heated to a constant and uniform temperature.
(c~ The catalyst bed temperature was raised to a temperature of 340-400C over a period of 15 to 30 minutes while a small flow of gaseous nitroyen was maintained through the reactor to aid in the removal of water vapor.
(d) A feed mixture containing HEP and water such that the organic component made up 60% of the mixture was then allowed to flow through the catalyst bed at a rate of 6.5-7.0 cc/hour; the nitrogen flow was discontinued.
(e) The catalyst bed temperature indicated in the tables set forth below was maintained during the run and the product samples were collected and analyzed. Analyses were performed using well-established gas chromatographic techniques.
The yields of TEDA and piperazine (PIP) as well as the conversion obtained from the catalysts of Examples 1-22 in Table 1 can be compared with those of Control Catalysts 1 and 3-5 in Table 2 below.
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v 1~84Z8 The results set forth in Table 1 where the catalysts of the examples demonstrate a unique ability to convert over 50 ~ol.% of the feed to prod-~cts the majority of which is TEDA. Depending on the particular feed stock, the yield of TEDA ranged from 6% in the worst case using Ni to approximately 84% in the best mode using 1 part SrHP04 to 3.5 parts BaHP04, see Example 1 above.
The former being the use of NiHPo4 with an aminoethyl-piperazine feed. When the feed over NiHPo4 was changed to hydroxyethylpiperazine, the yield increased 6 fold with a corresponding increase in the conversion from appro~imately 57% to 82%. The BaHPO4 catalysts per se did not meet the criteria for an effective catalyst for the conversion of HEP to TEDA. However, when approxi-mately four parts of this catalyst were combined withone part of SrHPO4 as in the Example 2, the yield of TEDA and the conversion increased based on a synergistic effect over that of the SrHPO4 catalyst.
Exam~le 63 The catalyst of Example 23 was tested in the conversion of crude HEP to TEDA. The reaction was carried out at atmospheric pressure, at a liquid hourly space velocity of 0.3 and at the temperatures indicated in Table 3 below.
Initial After 78 DaYs Bed Temp., C 360 368 HEP Conversion, wt. % g9+ 99+
TEDA Yield, wt. % 40.5 43.0 PIP Yield, wt. % 13.5 18.5 Example 64 The ca~alyst of Example 23 was tested for the conversion of diethanolamine to TEDA. The test was carried out at 370C using a feed consisting of diethan-11'9f342B
olamine and water (2.0 to 1.0 mole ratio) pumped intothe reactor at a rate of 4.4 liquid cc/hr along with helium diluent at a rate of 25 cc/minute. The diethanol-amine was in completely converted to TEDA, as the only, i.e. about 26 mol. %, recovered product.
Example 65 A 64% by weight solution of N-aminoethyl piperaæine in water was passed over a catalyst composition consisting essentially of SrHP04 at 380C and at a liquid hourly space velocity of 0.3 volumes of liquid per volume of catalyst. In a first pass operation there was obtained 96.8 mol. % conversion of the feed compound, obtaining a yield of 34.8% by weight (40.1 mol. %) TEDA and 27.1%
by weight ~40.6 mol. %) PIP.
Other typical condensation reactions in which SrHP04 may be employed as a catalyst include the formation of amines by amination of the corresponding alcohols with ammonia and the formation of polyamines from glycols and diamines.
It is believed that the key to the properties of the SrHP04 as a highly selective catalyst is due to the presence of a specific structure, which provides a narrow range of acidity. This narrow acidity range-displayed by SrHP04 may be optimum for promoting certain types of acid catalyzed reactions, in contrast to such catalysts as alumina, silica-alumina and the like which have acid sites of widely varying strength, and hence show relatively low selectivity for the desired reaction.
Example 65 Diethyleneglycol was passed over the SrHP04 catalyst of Example 23 in the presence of water at a temperature of 370C and at a contact time of 6.7 seconds. The feed contained 57 v~l. % diethyleneglycol and 43 vol.
% H20. The reaction product contained 33 wt. % 1,4-dioxane, corresponding to a yield of 47 mol. %.
The addition of water to the organic feeds may be desir~ble to prevent loss of catalyst activity as a result of dehydration of the SrHP04 to the pyrophosphate.
Example 67 The SrHP04 catalyst of Example 23 was tested for the conversion of 1, 4-butanediol to tetrahydrofuran.
The test was carried out at 350C using a feed consisting of 20 percent by volume of water and 80 percent by volume of 1, 4-butanediol pumped to the tubular reactor at a rate of 4.4 cc/hr. Helium dilutent was also fed at the rate of 30 cc/min. Under these conditions, the diol was completely converted to tetrahydrofuran.
Example 68 -The CaHP04 catalyst of Example 5 was recovered in a fine, powdered state and was deposited on inert alumina spheres instead of the silica-alumina spheres in the same manner as set forth under Example 3. 20 cc of the resulting coated alumina contained 2 gms. of CaHP04. The performance of this catalyst was evaluated for the preparation of an alipathic secondary amine with a feed mixture of monoethylamine (EA) and methanol using the general procedure used in Examples 25-62 for the preparation of TEDA. Specifically, 1 mol. of the primary amine and 1 mol. of the alcohol were reacted at 350C, 1 atmosphere pressure ancl an LHSV of 0.15/hr.
The conversion was 23.9 mol. % of the ME to the secondary aliphatic amine. The yield of methylethylamine (MEA) was 16.5 mol. % of the amine feed with a selectivity of 69 mol. %. The only oth~r product in any significant c~antity was dimethylethylamine (DMEA) with a yield of 5.4 mol. % and a selectivity of 22 mol %.
34~
Example 69 The procedure of Example 68 was followed except that 1 mol. of die~lylamine (DEA) was substituted for 1 mol. of EA. 27.6 mol. % of this primary amine in the feed was convexted for the most part to a single secondary ~mine, i.e. diethylmethylamine (DEMA) and a trace amount of a tertiary amine, i.e. triethylamine. The yield of DEA fed was 23 mol. % DEMA with a selectivity of 83.3 mol. %.
Examples 70-71 3 grams of the La2(HP04)3 catalyst of Example 9 were coated onto alurnina spheres and the procedures of Example 60 and 69 were followed. The results from these reactions are summarized in Table 4 below.
Examples 72-73 The SrHP04 catalyst of Example 6, was used to convert methanol and either monoethylamine (Example 72) or diethylamine (Example 73) in the same manner set forth under Example 68.
The results of these Examples 72-73 are summarized and compared with the other Examples 68-71 in Table 4 below.
ALIPHATIC AMINE PROD~CTION
Amine Yield, mol. % Selectivity, Mol. % Conversion Feed MEA DMEA DEMA MEA DMEA DEMA _ Mol. %
Example 68 EA 16.5 5.4 - 69 22 - 23.9 69 DEA - - 23 - - 83.3 27.6 73 DEA 1.4 6.9 41 2.8 13.8 82 50 ~7) Dimethylethylamine.
~8~2~3 The data of Table 4 above illustrates the unexpect-edly high selectivities to the corresponding aliphatic amine without the formation of the corresponding by-products of thermodynamic amine equilibration. The relatively low conversion to product of Examples 6B-71 can be attributed to the fact that only 2 gms. of CaHPO4 or 3 gms. La2(HPO4)3 were used in Examples 68-71 in comparison to about 20 gms. of SrHP04 that were used in Examples 72 and 73.
Example 74 The CuHPO4 catalyst of Example 13 was coated onto alumina spheres and the procedure of Example 68 was followed except that 1 mol. of a~onia was substituted for 1 mol. of EA. The results from this reaction were a 65 mol. % yield of monomethylamine (MA) based on the methanol, an 87 mol.% selectivity to MA and a methanol conversion of 75 mol. %.
ExamPle 75 The La2(HPO4~3 catalyst of Example 9 was deposited on alumina spheres and the procedure of Example 74 was followed. The results were yields based on the methanol in the feed of 13 mol. % trimethylamine (TMA), 2.8 mol.
% dimethylamine (DMA) and 3 mol. % monomethylamine (MA), selectivities based on the methanol of 69 mol. %
TMA, 14.9 mol. % DMA and 16 mol. % MA, and a methanol conversion of 52 mol. %.
It has also been found that MgHPO4 and BaHPO4 were effective in selectivity converting amines to the corresponding higher molecular weight amine.
Examples 76-82 ~ he ~Sr-Ni)HPO4 catalyst of Example 24 was evaluated for the preparation of N-(2-dimethylaminoethyl)morpholine ~DMAEM) with a feed mixture of morpholine (MOR), dimethyl-2~3 ethanolamine (DMEA), distilled water, hydrogen andhelium in the amounts shown below in Table 5 using the general procedure used in Examples 25-62 for the TEDA
preparation. Specifically the condensation reaction was carried out at 340C, 1 atmosphere of pressure and an LHSV in the range of 0.31-0.44~1r. as shown in Table 5 in the presence of 20 cc. of the (Sr-Ni)HPC4 catalyst granules.
Examples 83-86 The SrHPO4 catalyst of Example 6 was used in place of the (Sr-Ni)HPO4 catalyst of Example 24 and the condensation reactions were carried out in the same manner as described under Examples 76-82. The results of these runs are summarized and compared with the Examples 76-82 feed, yield and conversion data in Table 5 below.
DMAEM PRODUCTION
Example Feed, LHSV, Yield, Mol. % Conversion, 20 _ Vol. % hr. MOR Mol. %
76 MOR 60 , 0.31 100 16 H2e (20 cc/min) H2 (20 cc/min) 77 MOR 60 0.44 63 23 He (20 cc/min) H2 (20 cc/min) 78 MOR 40 0.31 53 43 He (20 cc/min) H2 (20 cc/min) ~9~34Z~
TABLE 5 - (Cont'd) DMAEM PRODUCTION
Example Feed, LHSV, Yield, Mol. % onversion, Vol. %h -1 MOR Mol. %
79 MOR 40 0.21 58 48 He (20 cc/min) H2 (20 cc/min) MOR 20 0.31 52 60 He (20 cc/min) H2 (20 cc/min) 81 MOR 20 0.21 58 75 He (20 cc/min) H2 ~20 cc/min) 82 MOR 40 0.31 97 21 H2e (20 cc/min) H2 (20 cc/min) 83 MOR 40 0.21 42 32 He (20 cc/min) 84 MOR 40 0.21 37 28 He (20 cc/min) MOR 60 0.21 43 22 H2O ~
He (20 cc/min) 86 MOR 20 0.21 33 45 H2e (20 cc/min) 42~
~7 Examples 87-91 The catalyst product of Example 1 was evaluated for cataly-tic performance for the preparation of morpho-line from diglycolamine at 1 atmosphere in accordance with the following test procedure:
(a) 10 cc (approximately 3.1 g.) of Sr~O4 was loaded into a 3/4 " diameter stainless steel reactor.
(b) The reactor was placed in a conventional tube furnace such that the catalyst bed was near the furnace center and therefore could be heated to a constant and uniform temperature.
(c) The catalyst bed temperature was slowly raised to a temperature of 250C over a period of 15 to 30 minutes while a small flow of gaseous helium was maintained through the reactor in three of the examples.
(d) A feed mixture containing DGA and water (excépt for Examples 88 and 90) in the ratio set forth in Table 6 below was then allowed to flow through the catalys-t bed at an LHSV of 0.21 to 0.88; the helium flow was continued through the run ~except for Examples 90-91).
(e) The catalyst bed temperature indicated in Table 6 below were maintained throughout -the run and the product samples were collected and analyzed. Analyses were performed using well-established gas chromatographic techniques.
The operating conditions and yields obtained from the catalyst of Example 1 are summarized in Table 6 below.
342~
Table 6 Example 87 88 89 90 91 F~ed, DGA/H20, Vol. % 80/20100~080/20 100/0 50/50 Helium Diluent, cc/min. 34.5 34 28.5 None None Temp., C 320 320 370 350 330 Contact Time, sec. 12 55 12 13 22 LHSV 0.21 0.21 0.44 0.88 0.21 Yield of Morpholine, mol. ~ 85 63 37 46 75 Selectivity to Mo~pholine % 85 74 37 57.5 75.6 Conv. of DGA mol. %100 85 100 80 99 Dioxane Yield, mol. % ~-- less than 1%
In each of the Examples 87-91, it was unexpectedly found that DGA could be to selectively converted to morpholine without the conversion of appreciable quantities of dioxane, tar or other high molecular weight components.
It would be expected that the reaction product from DGA
conversion would contain substantially equal amounts of dioxane and morpholine.
~, ` Examples 92-118 - The test procedure set forth in Examples 87-91 was followed in Examples 92~118 in the presence of the Example 1 catalyst. Table 7 below sets forth the feed mixture, operating conditions and the product yields fQr each example.
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Control 4 200 grams of Sr(NO3~2 were dissolved in distilled water and diluted to 400 cc. 92 grams of H2SO4 were diluted in 200 cc. of distilled H20 75 grams of 50 wt. % NaOH solution were diluted to 200 cc. with distilled water. The H2SO~ and NaOH solutions were mixed together slowly. ~he Sr(N03)2 solution was stirred into the solution containing H2SO4 and NaOH. The solution was stirred for 10 minutes and the precipitate was filtered, washed and dried. The surface pH of the resulting catalyst was less than 3 which was believed to be substantially all SrSO4.
Example 17 71 grams of Na2HP04 were dissolved in 500 cc. of distilled water. 101.7 grams of MgC12.6H20 were dis-solved in 500 cc. of distilled H2O. Both solutions were mixed together and the precipitate was filtered, washed and dried. The surface pH of the MgHPO4 product was 7-8.
Example 18 71 grams of Na2HP04 and 130.7 grams of Ba(NO3)2 were each separately dissolved in 500 cc. of distilled H2O The 2 solutions were mixed and the precipitate was filtered, washed and dried. The resulting BaHP04 had a surface pH of 8-9.
2~
Each of the products resulting from the procedures of Examples 17 and 18 above were coated on the silica-alumina spheres in the same manner as indicated in Example 3.
Example 19 The SrHP04 catalyst of Example 6 was heat treated for 2 hours in the presence of a mixture 20% by volume steam and the balance air at 350C. The resulting strontium pyrophosphate (Sr2P2O7) had a crushing strength of 0.47 kg./mm of length and a packed bulk density of 1.01 kg./l.
ExamPle 20 The ZnHP04 catalyst product of Example 14 above was coated on the silica-alumina spheres in the manner set forth in Example 3.
Example 21 132.5 grams of strontium hydroxide octahydrate --Sr(OH)2.8H2O-- were dissolved in a solution of 750 cc. of 85% phosphoric acid and 1500 cc. of distilled water. The resulting solution was slowly evaporated to a total volume of about 900 cc. with the temperature being maintained at 25 to 30~C. The solution was cooled to 5C overnight and a whi-te precipitate was recovered by vacuum filtration. The resulting Sr(H2PO4)2 precipitate was washed with 5-300 cc. portions of anhydrous ethanol and with 2-200 cc. portions of anhy-drous ether. The product was dried at room temperature under vacuum for 6 hours. An elemental analysis of the product showed a P/Sr mol ratio of 2.04 and the surface pH was found to be 0.2-1.2. The fine powder was pressed into tablets the size of a typical"Aspirin" (registered trade mark) tablet and crushed to granules 1~8 to 1/4 inch in size.
34Z~
Example 2_ The fine powder of the catalyst prepared in accor-dance with Example 21 was deposited on silica-alumina spheres in the manner set forth in Example 3.
Example 23 2000 grams of Sr~NO3)2 were dissolved in 2000 cc -, of deionized water and the solution diluted to 4000 cc with deionized water after dissolution of the Sr(N03)2 was complete.
In another container, 1342.3 grams of Na2HP04 were dissolved in 2000 cc of deionized water. After solution of the na2HP04 was complete, the solution was diluted to 4000 cc with deionized water. The pH of this solution was approximately 8.~3.
Precipitation of SrHP04 was effected by slowly adding the Na2HP04 solution to the Sr(NO3)2 solution with rapid stirring. The white SrHP04 precipitated rapidly from solution forming a rather thick slurry.
This slurry was mixed for one hour, after which time the pH ~as measured to be about six.
The solid SrHP04 was recovered by filterir.g on an eight frame filter press using cloth filters. It was washed with deionized water. After filtering and washing, the solid was dried in a circulating hot air oven at 250F for four hours. The yield of SrHPO4 was 1680 grams. The solid was wetted and formed into pellets by extrusion through a 3.1 mm die plate and cutting the extrudates to about 1/4 inch in length.
After drying the extrudate at 250F for four hours in a circulating hot air oven, they were heat treated at 662F for two hours in a 20% steam, 80% air atmosphere.
Example 24 106 grams o~ Sr(N03)2 and 145 grams of Ni (N03)2 6H2O were dissolved in distilled water and diluted to ~9~342~3 500 cc. 132 grams of (NH4)2HP04 were dissolved in distilled water and diluted to 50~ cc. the remaini~g steps of Example 1 were carried out to yield a ~Sr-Ni)HPO4 catalyst having a surface pH of 5.4-7Ø
USE OF CATAL~STS
Examples 25-62 Each o~ the prcducts prepared in accordance with Examples 1 through 22 and Controls 1 and 3-5 above were evaluated for catalytic performance for the preparation of TEDA with either a feed mixture containing hydroxy-ethylpiperazine (HEP) or N-aminoethylpiperazine (AEP) in accordance with the following test procedure:
(a) 20 cc (approximately 6.2g.) of the catalyst was loaded into a 3/4 " diameter stainless steel reactor.
(b) The reactor was placed in a conventional tube furnace such that the catalyst bed was near the furnace center and therefore could be heated to a constant and uniform temperature.
(c~ The catalyst bed temperature was raised to a temperature of 340-400C over a period of 15 to 30 minutes while a small flow of gaseous nitroyen was maintained through the reactor to aid in the removal of water vapor.
(d) A feed mixture containing HEP and water such that the organic component made up 60% of the mixture was then allowed to flow through the catalyst bed at a rate of 6.5-7.0 cc/hour; the nitrogen flow was discontinued.
(e) The catalyst bed temperature indicated in the tables set forth below was maintained during the run and the product samples were collected and analyzed. Analyses were performed using well-established gas chromatographic techniques.
The yields of TEDA and piperazine (PIP) as well as the conversion obtained from the catalysts of Examples 1-22 in Table 1 can be compared with those of Control Catalysts 1 and 3-5 in Table 2 below.
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v 1~84Z8 The results set forth in Table 1 where the catalysts of the examples demonstrate a unique ability to convert over 50 ~ol.% of the feed to prod-~cts the majority of which is TEDA. Depending on the particular feed stock, the yield of TEDA ranged from 6% in the worst case using Ni to approximately 84% in the best mode using 1 part SrHP04 to 3.5 parts BaHP04, see Example 1 above.
The former being the use of NiHPo4 with an aminoethyl-piperazine feed. When the feed over NiHPo4 was changed to hydroxyethylpiperazine, the yield increased 6 fold with a corresponding increase in the conversion from appro~imately 57% to 82%. The BaHPO4 catalysts per se did not meet the criteria for an effective catalyst for the conversion of HEP to TEDA. However, when approxi-mately four parts of this catalyst were combined withone part of SrHPO4 as in the Example 2, the yield of TEDA and the conversion increased based on a synergistic effect over that of the SrHPO4 catalyst.
Exam~le 63 The catalyst of Example 23 was tested in the conversion of crude HEP to TEDA. The reaction was carried out at atmospheric pressure, at a liquid hourly space velocity of 0.3 and at the temperatures indicated in Table 3 below.
Initial After 78 DaYs Bed Temp., C 360 368 HEP Conversion, wt. % g9+ 99+
TEDA Yield, wt. % 40.5 43.0 PIP Yield, wt. % 13.5 18.5 Example 64 The ca~alyst of Example 23 was tested for the conversion of diethanolamine to TEDA. The test was carried out at 370C using a feed consisting of diethan-11'9f342B
olamine and water (2.0 to 1.0 mole ratio) pumped intothe reactor at a rate of 4.4 liquid cc/hr along with helium diluent at a rate of 25 cc/minute. The diethanol-amine was in completely converted to TEDA, as the only, i.e. about 26 mol. %, recovered product.
Example 65 A 64% by weight solution of N-aminoethyl piperaæine in water was passed over a catalyst composition consisting essentially of SrHP04 at 380C and at a liquid hourly space velocity of 0.3 volumes of liquid per volume of catalyst. In a first pass operation there was obtained 96.8 mol. % conversion of the feed compound, obtaining a yield of 34.8% by weight (40.1 mol. %) TEDA and 27.1%
by weight ~40.6 mol. %) PIP.
Other typical condensation reactions in which SrHP04 may be employed as a catalyst include the formation of amines by amination of the corresponding alcohols with ammonia and the formation of polyamines from glycols and diamines.
It is believed that the key to the properties of the SrHP04 as a highly selective catalyst is due to the presence of a specific structure, which provides a narrow range of acidity. This narrow acidity range-displayed by SrHP04 may be optimum for promoting certain types of acid catalyzed reactions, in contrast to such catalysts as alumina, silica-alumina and the like which have acid sites of widely varying strength, and hence show relatively low selectivity for the desired reaction.
Example 65 Diethyleneglycol was passed over the SrHP04 catalyst of Example 23 in the presence of water at a temperature of 370C and at a contact time of 6.7 seconds. The feed contained 57 v~l. % diethyleneglycol and 43 vol.
% H20. The reaction product contained 33 wt. % 1,4-dioxane, corresponding to a yield of 47 mol. %.
The addition of water to the organic feeds may be desir~ble to prevent loss of catalyst activity as a result of dehydration of the SrHP04 to the pyrophosphate.
Example 67 The SrHP04 catalyst of Example 23 was tested for the conversion of 1, 4-butanediol to tetrahydrofuran.
The test was carried out at 350C using a feed consisting of 20 percent by volume of water and 80 percent by volume of 1, 4-butanediol pumped to the tubular reactor at a rate of 4.4 cc/hr. Helium dilutent was also fed at the rate of 30 cc/min. Under these conditions, the diol was completely converted to tetrahydrofuran.
Example 68 -The CaHP04 catalyst of Example 5 was recovered in a fine, powdered state and was deposited on inert alumina spheres instead of the silica-alumina spheres in the same manner as set forth under Example 3. 20 cc of the resulting coated alumina contained 2 gms. of CaHP04. The performance of this catalyst was evaluated for the preparation of an alipathic secondary amine with a feed mixture of monoethylamine (EA) and methanol using the general procedure used in Examples 25-62 for the preparation of TEDA. Specifically, 1 mol. of the primary amine and 1 mol. of the alcohol were reacted at 350C, 1 atmosphere pressure ancl an LHSV of 0.15/hr.
The conversion was 23.9 mol. % of the ME to the secondary aliphatic amine. The yield of methylethylamine (MEA) was 16.5 mol. % of the amine feed with a selectivity of 69 mol. %. The only oth~r product in any significant c~antity was dimethylethylamine (DMEA) with a yield of 5.4 mol. % and a selectivity of 22 mol %.
34~
Example 69 The procedure of Example 68 was followed except that 1 mol. of die~lylamine (DEA) was substituted for 1 mol. of EA. 27.6 mol. % of this primary amine in the feed was convexted for the most part to a single secondary ~mine, i.e. diethylmethylamine (DEMA) and a trace amount of a tertiary amine, i.e. triethylamine. The yield of DEA fed was 23 mol. % DEMA with a selectivity of 83.3 mol. %.
Examples 70-71 3 grams of the La2(HP04)3 catalyst of Example 9 were coated onto alurnina spheres and the procedures of Example 60 and 69 were followed. The results from these reactions are summarized in Table 4 below.
Examples 72-73 The SrHP04 catalyst of Example 6, was used to convert methanol and either monoethylamine (Example 72) or diethylamine (Example 73) in the same manner set forth under Example 68.
The results of these Examples 72-73 are summarized and compared with the other Examples 68-71 in Table 4 below.
ALIPHATIC AMINE PROD~CTION
Amine Yield, mol. % Selectivity, Mol. % Conversion Feed MEA DMEA DEMA MEA DMEA DEMA _ Mol. %
Example 68 EA 16.5 5.4 - 69 22 - 23.9 69 DEA - - 23 - - 83.3 27.6 73 DEA 1.4 6.9 41 2.8 13.8 82 50 ~7) Dimethylethylamine.
~8~2~3 The data of Table 4 above illustrates the unexpect-edly high selectivities to the corresponding aliphatic amine without the formation of the corresponding by-products of thermodynamic amine equilibration. The relatively low conversion to product of Examples 6B-71 can be attributed to the fact that only 2 gms. of CaHPO4 or 3 gms. La2(HPO4)3 were used in Examples 68-71 in comparison to about 20 gms. of SrHP04 that were used in Examples 72 and 73.
Example 74 The CuHPO4 catalyst of Example 13 was coated onto alumina spheres and the procedure of Example 68 was followed except that 1 mol. of a~onia was substituted for 1 mol. of EA. The results from this reaction were a 65 mol. % yield of monomethylamine (MA) based on the methanol, an 87 mol.% selectivity to MA and a methanol conversion of 75 mol. %.
ExamPle 75 The La2(HPO4~3 catalyst of Example 9 was deposited on alumina spheres and the procedure of Example 74 was followed. The results were yields based on the methanol in the feed of 13 mol. % trimethylamine (TMA), 2.8 mol.
% dimethylamine (DMA) and 3 mol. % monomethylamine (MA), selectivities based on the methanol of 69 mol. %
TMA, 14.9 mol. % DMA and 16 mol. % MA, and a methanol conversion of 52 mol. %.
It has also been found that MgHPO4 and BaHPO4 were effective in selectivity converting amines to the corresponding higher molecular weight amine.
Examples 76-82 ~ he ~Sr-Ni)HPO4 catalyst of Example 24 was evaluated for the preparation of N-(2-dimethylaminoethyl)morpholine ~DMAEM) with a feed mixture of morpholine (MOR), dimethyl-2~3 ethanolamine (DMEA), distilled water, hydrogen andhelium in the amounts shown below in Table 5 using the general procedure used in Examples 25-62 for the TEDA
preparation. Specifically the condensation reaction was carried out at 340C, 1 atmosphere of pressure and an LHSV in the range of 0.31-0.44~1r. as shown in Table 5 in the presence of 20 cc. of the (Sr-Ni)HPC4 catalyst granules.
Examples 83-86 The SrHPO4 catalyst of Example 6 was used in place of the (Sr-Ni)HPO4 catalyst of Example 24 and the condensation reactions were carried out in the same manner as described under Examples 76-82. The results of these runs are summarized and compared with the Examples 76-82 feed, yield and conversion data in Table 5 below.
DMAEM PRODUCTION
Example Feed, LHSV, Yield, Mol. % Conversion, 20 _ Vol. % hr. MOR Mol. %
76 MOR 60 , 0.31 100 16 H2e (20 cc/min) H2 (20 cc/min) 77 MOR 60 0.44 63 23 He (20 cc/min) H2 (20 cc/min) 78 MOR 40 0.31 53 43 He (20 cc/min) H2 (20 cc/min) ~9~34Z~
TABLE 5 - (Cont'd) DMAEM PRODUCTION
Example Feed, LHSV, Yield, Mol. % onversion, Vol. %h -1 MOR Mol. %
79 MOR 40 0.21 58 48 He (20 cc/min) H2 (20 cc/min) MOR 20 0.31 52 60 He (20 cc/min) H2 (20 cc/min) 81 MOR 20 0.21 58 75 He (20 cc/min) H2 ~20 cc/min) 82 MOR 40 0.31 97 21 H2e (20 cc/min) H2 (20 cc/min) 83 MOR 40 0.21 42 32 He (20 cc/min) 84 MOR 40 0.21 37 28 He (20 cc/min) MOR 60 0.21 43 22 H2O ~
He (20 cc/min) 86 MOR 20 0.21 33 45 H2e (20 cc/min) 42~
~7 Examples 87-91 The catalyst product of Example 1 was evaluated for cataly-tic performance for the preparation of morpho-line from diglycolamine at 1 atmosphere in accordance with the following test procedure:
(a) 10 cc (approximately 3.1 g.) of Sr~O4 was loaded into a 3/4 " diameter stainless steel reactor.
(b) The reactor was placed in a conventional tube furnace such that the catalyst bed was near the furnace center and therefore could be heated to a constant and uniform temperature.
(c) The catalyst bed temperature was slowly raised to a temperature of 250C over a period of 15 to 30 minutes while a small flow of gaseous helium was maintained through the reactor in three of the examples.
(d) A feed mixture containing DGA and water (excépt for Examples 88 and 90) in the ratio set forth in Table 6 below was then allowed to flow through the catalys-t bed at an LHSV of 0.21 to 0.88; the helium flow was continued through the run ~except for Examples 90-91).
(e) The catalyst bed temperature indicated in Table 6 below were maintained throughout -the run and the product samples were collected and analyzed. Analyses were performed using well-established gas chromatographic techniques.
The operating conditions and yields obtained from the catalyst of Example 1 are summarized in Table 6 below.
342~
Table 6 Example 87 88 89 90 91 F~ed, DGA/H20, Vol. % 80/20100~080/20 100/0 50/50 Helium Diluent, cc/min. 34.5 34 28.5 None None Temp., C 320 320 370 350 330 Contact Time, sec. 12 55 12 13 22 LHSV 0.21 0.21 0.44 0.88 0.21 Yield of Morpholine, mol. ~ 85 63 37 46 75 Selectivity to Mo~pholine % 85 74 37 57.5 75.6 Conv. of DGA mol. %100 85 100 80 99 Dioxane Yield, mol. % ~-- less than 1%
In each of the Examples 87-91, it was unexpectedly found that DGA could be to selectively converted to morpholine without the conversion of appreciable quantities of dioxane, tar or other high molecular weight components.
It would be expected that the reaction product from DGA
conversion would contain substantially equal amounts of dioxane and morpholine.
~, ` Examples 92-118 - The test procedure set forth in Examples 87-91 was followed in Examples 92~118 in the presence of the Example 1 catalyst. Table 7 below sets forth the feed mixture, operating conditions and the product yields fQr each example.
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Claims (30)
1. In a method for the synthesis of an organic amine com-pound, the improvement which comprises subjecting said amine compound to a condensation reaction in the presence of a cata-lyst selected from the group consisting of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, sub-ject to the exclusion of the pyrophosphate, monohydrogen phos-phate and dihydrogen phosphate of strontium per se, and mix-tures thereof
2. The method as defined in claim 1 wherein said cata-lyst is associated with a carrier of the group consisting of silica, alumina and silica-alumina.
3. In a method for the synthesis of an organic amine by reacting an alcohol with an amine or ammonia in the presence of phosphate catalysts, the improvement for enhanced activity and selectivity which comprises using a catalyst selected from the group consisting of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, cal-cium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclu-sion of the pyrophosphate, monohydrogen phosphate and dihy-drogen phosphate of strontium per se, and mixtures thereof.
4. The method as defined in claim 3 wherein said cata-lyst is associated with a carrier of the group consisting of silica, alumina and silica-alumina.
5. The method as defined in claim 1 wherein the amine is subjected to a condensation reaction resulting in the elimina-tion of water.
6. The method as defined in claim 1 wherein the amine is subjected to a condensation reaction resulting in the elimina-tion of ammonia.
7. The method as defined in claim 1 or 2 wherein the amine is subjected to a condensation reaction effecting cycliza-tion.
8. The method as defined in claim 1 wherein hydroxyethyl-piperazine is subjected to said condensation reaction to form triethylenediamine.
9. The method as defined in claim 1 wherein crude hydroxyethylpiperazine is subjected to said condensation reac-tion to form triethylenediamine.
10. The method as defined in claim 1 wherein said reac-tion comprises reacting ethanolamines to form triethylene-diamine.
11. The method as defined in claim 1 wherein N-aminoethyl-piperazine is subjected to said condensation reaction to form triethylenediamine.
12. The method as defined in claim 1 wherein said conden-sation reaction comprises reacting an alcohol and an amine or ammonia to form an aliphatic or aromatic amine.
13. The method as defined in claim 1 or 2 wherein said reaction takes place in the presence of an inert gas.
14. The method as defined in claim 8, 9 or 11 wherein the reaction is carried out in the presence of water.
15. The method as defined in claim 1 or 2, wherein the reaction is carried out in the presence of water.
16. A method which comprises converting a substituted piperazine compound selected from the group consisting of hydroxyethylpiperazine and aminoethylpiperazine to triethylene-diamine at a temperature in the range of about 285°C to 420°C, a liquid hourly space velocity of about 0.05 to 1.5 in the presence of a catalyst selected from the group consisting of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclusion of the pyrophos-phate, monohydrogen phosphate and dihydrogen phosphate of stron-tium per se, and mixtures thereof.
17. A method which comprises converting hydroxyethylpiper-azine to greater than 50 mol.% yield of triethylenediamine at a temperature in the range of about 340°C to 400°C, a liquid hourly space velocity of about 0.1 to 0.3 in the presence of a catalyst selected from the group consisting of the pyrophos-phate, monohydrogen phosphate and dihydrogen phosphate of strontium, calcium, magnesium, zinc, mixtures of strontium and barium in the ratio of Sr to Ba of 1 to 5 to 5 to 1 and mix-tures of lanthanum and strontium in the ratio of La to Sr of 15 to 1 to 1 to 15, subject to the exclusion of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium per se, and mixtures thereof.
18. A method which comprises converting a nitrogen-containing compound selected from the group consisting of ammonia, primary and secondary aliphatic amines and aromatic amines to its corresponding symmetrical and unsymmetrical higher molecular weight aliphatic or aromatic amine in the presence of an alcohol at a temperature in the range of about 285°C to 420°C, a liquid hourly space velocity of about 0.1 to 1.5 in the presence of a catalyst selected from the group consisting of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclusion of the pyrophosphate, monohydrogen phosphate and dihydrogen phos-phate of strontium per se, and mixtures thereof.
19. A method which comprises selectively converting greater than 50 mol.% of a nitrogen-containing compound se-lected from the group consisting of ammonia, primary and second-ary aliphatic amines and aromatic amines having 1 to 20 carbon atoms per molecule to its corresponding higher molecular weight aliphatic or aromatic amine in the presence of an alcohol hav-ing 1 to 20 carbon atoms per molecule in the molar ratio of said nitrogen-containing compound to alcohol in the range of about 6 to 1 to 1 to 6 at a temperature in the range of about 340°C to 400°C, a liquid hourly space velocity of 0.1 to 0.3 in the presence of a catalyst selected from the group consist-ing of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, lanthanum, and mixtures thereof, subject to the exclusion of the pyrophosphate, monohydrogen phosphate and dihydrogen phos-phate of strontium per se, and mixtures thereof.
20. A method which comprises converting morpholine and dimethylethanolamine to dimethylaminoethylmorpholine in the presence of water and hydrogen at a temperature in the range of about 285°C to 420°C, a liquid hourly space velocity of about 0.05 to 1.5 in the presence of a catalyst selected from the group consisting of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, cal-cium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclu-sion of the pyrophosphate, monohydrogen phosphate and dihy-drogen phosphate of strontium per se, and mixtures thereof.
21. The method as defined in claim 20, wherein an inert gas is present during the conversion.
22. A method which comprises converting morpholine and dimethylethanolamine in the molar ratio of morpholine to dimethylethanolamine of about 1 to 3 to 3 to 1 in the presence of water, hydrogen and an inert gas to greater than 50 mol.%
yield of dimethylaminoethylmorpholine at a temperature in the range of about 360°C to 400°C, a liquid hourly space velo-city of about 0.1 to 0.3 in the presence of a mixed nickel and strontium hydrogen phosphate catalyst.
yield of dimethylaminoethylmorpholine at a temperature in the range of about 360°C to 400°C, a liquid hourly space velo-city of about 0.1 to 0.3 in the presence of a mixed nickel and strontium hydrogen phosphate catalyst.
23. A method which comprises converting a diglycolamine compound to a morpholine compound at a temperature in the range of about 285°C to 420°C, a liquid hourly space velocity of about 0.05 to 1.5 in the presence of a catalyst selected from the group consisting of the pyrophosphate, monohydrogen phos-phate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclu-sion of the pyrophosphate, monohydrogen phosphate and dihy-drogen phosphate of strontium per se, and mixtures thereof.
24. The method of claim 23 wherein the conversion takes place in the presence of an inert gas.
25. The method of claim 23 wherein said diglycolamine com-pound is selected from the group consisting of diglycolamine and alkyl diglycolamine and mixtures thereof and said morpho-line compound is selected from the group consisting of morpho-line and alkyl morpholine and mixtures thereof, wherein each of said alkyl groups contains from 1 to 6 carbon atoms.
26. A method which comprises converting diglycolamine to morpholine at a temperature in the range of about 285°C to 420°C, a liquid hourly space velocity of about 0.05 to 1.5 in the presence of a catalyst selected from the group consisting of the pyrophosphate, monohydrogen phosphate and dihydrogen phosphate of strontium, copper, magnesium, calcium, barium, zinc, lanthanum, aluminum, cobalt, nickel, cerium, neodymium, and mixtures thereof, subject to the exclusion of the pyrophos-phate, monohydrogen phosphate and dihydrogen phosphate of stron-tium per se, and mixtures thereof.
27. The method as defined in claim 26 wherein the conver-sion is carried out in the presence of water.
28. The method as defined in claim 26 or 27 wherein the conversion takes place in the presence of an inert gas.
29. The method as defined in claim 1, 2 or 3, wherein the catalyst is selected from the group consisting of strontium dihydrogen phosphate, lanthanum mono- or dihydrogen phosphate, cerium, neodymium, and mixtures thereof including mixtures of such compounds with strontium monohydrogen phosphate.
30. The method as defined in claim 4 or 12, wherein the catalyst is selected from the group consisting of strontium dihydrogen phosphate, lanthanum mono- or dihydrogen phosphate, cerium, neodymium, and mixtures thereof including mixtures of such compounds with strontium monohydrogen phosphate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000444540A CA1198429A (en) | 1982-05-24 | 1983-12-30 | Catalysis of condensation reactions |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/381,233 US4501889A (en) | 1982-05-24 | 1982-05-24 | Morpholine compounds prepared via phosphate catalysts |
| US381,232 | 1982-05-24 | ||
| US381,233 | 1982-05-24 | ||
| US06/381,232 US4521600A (en) | 1982-05-24 | 1982-05-24 | Triethylenediamine preparation via phosphate catalysts |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000444540A Division CA1198429A (en) | 1982-05-24 | 1983-12-30 | Catalysis of condensation reactions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1198428A true CA1198428A (en) | 1985-12-24 |
Family
ID=27009299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000405618A Expired CA1198428A (en) | 1982-05-24 | 1982-06-21 | Catalysis of condensation reactions |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1198428A (en) |
-
1982
- 1982-06-21 CA CA000405618A patent/CA1198428A/en not_active Expired
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