CA1060424A - Alumina-based bodies obtained by agglomeration which are resistant to elevated temperatures - Google Patents
Alumina-based bodies obtained by agglomeration which are resistant to elevated temperaturesInfo
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- CA1060424A CA1060424A CA217,700A CA217700A CA1060424A CA 1060424 A CA1060424 A CA 1060424A CA 217700 A CA217700 A CA 217700A CA 1060424 A CA1060424 A CA 1060424A
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- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/10—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of rare earths
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
- B01J20/08—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/12—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of actinides
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
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- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
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- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
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Abstract
ALUMINA-BASED BODIES OBTAINED BY AGGLOMERATION
WHICH ARE RESISTANT TO ELEVATED TEMPERATURES
ABSTRACT OF THE DISCLOSURE
Alumina based bodies having resistance to temperatures of up to 1200°C prepared by autoclaving alumina and at least one additive from the group of oxides of lanthanum, neodymium, praseodymium and thorium. Bodies of the alumina of this invention are useful in adsorption and catalysis.
WHICH ARE RESISTANT TO ELEVATED TEMPERATURES
ABSTRACT OF THE DISCLOSURE
Alumina based bodies having resistance to temperatures of up to 1200°C prepared by autoclaving alumina and at least one additive from the group of oxides of lanthanum, neodymium, praseodymium and thorium. Bodies of the alumina of this invention are useful in adsorption and catalysis.
Description
The invention relates to alumina-based substances obtained by agglomeration of active alumina, whose resis-tance at high temperatures is increased by the addition o~
metallic oxides.
It is well known that the agglomeration of particles of active alumina gives substances which find very diverse applications, and that greatly varied characteristics of speci~ic surface and porosity can be imparted to these substances according to the desired applications or uses, which are particularly important in adsorption and catalysis.
However, these characteristics are not the only ones to be considered since these substances, in order to be capable of industrial use, must possess good properties of mechanical resistance, both to crushing and to attrition.
Moreover, it is very frequent that in the course of their use or in the course of regeneration operations, such substances obtained by agglomeration are subjected to tem-peratures which are sufficiently high to cause a change or alteration in their texture and structure. That modifies ~20 not only their adsorbent or catalytic properties but li~ewise their machanical properties; these latter proper-ties, being a function of the-temperature, in fact, gen-erally pass through a minimum associated with the progres-sive loss of water molecules entering contained in the various active aluminas, the cohesion of the different alumina parti~les then increasing by supplementary raising of the ~emperature which involves fritting of these particles which are then in the state of C~ alumina or corundum.
Numerous experiments have been carried out in order 3~, to cbtain alumina-based materials which retain great ~L
q~
metallic oxides.
It is well known that the agglomeration of particles of active alumina gives substances which find very diverse applications, and that greatly varied characteristics of speci~ic surface and porosity can be imparted to these substances according to the desired applications or uses, which are particularly important in adsorption and catalysis.
However, these characteristics are not the only ones to be considered since these substances, in order to be capable of industrial use, must possess good properties of mechanical resistance, both to crushing and to attrition.
Moreover, it is very frequent that in the course of their use or in the course of regeneration operations, such substances obtained by agglomeration are subjected to tem-peratures which are sufficiently high to cause a change or alteration in their texture and structure. That modifies ~20 not only their adsorbent or catalytic properties but li~ewise their machanical properties; these latter proper-ties, being a function of the-temperature, in fact, gen-erally pass through a minimum associated with the progres-sive loss of water molecules entering contained in the various active aluminas, the cohesion of the different alumina parti~les then increasing by supplementary raising of the ~emperature which involves fritting of these particles which are then in the state of C~ alumina or corundum.
Numerous experiments have been carried out in order 3~, to cbtain alumina-based materials which retain great ~L
q~
-2-mechanical resistance at quite high temperatures, and are nevertheless endowed with the desired characteristics of specific surface and porosity. With this aim, for example~ -it has been proposed to autoclave substances obtained by agglomeration of active alumina particles, the effect being particularly marked when this treatment takes place in the presence of various acids. These processes lead to satis-factory results, and the substances thus obtained are particularly well suited for use in certain catalytic applications such as the purification of the gases emitted by internal combustion engines, where temperatures between 1000 and 1100C, or even 1200C, are reached. The specific surface of these substances are moderate but their porosity should be quite high. Such processes are described in ~15 Fxench Patents ~os. 1,386,364 and 1,449,904.
Another way to avoid the progressive transformation -of active aluminas by loss of water at high temperatures comprises adding various oxides thereto which act as stabilizers. With this aim, the most frequently recommended oxides are those of the alkaline and alkaline earth metals, oxides of the metals of Group III A of the periodic table, oxides of thorium and oxides of silicon. However, the instructions given in the past are frequently of too general a nature to permit preparation, wi*h certainty, of suffi-ciently interesting results for industrial exploitation,and, furthermore, certain recommended additives can inter-fere harmfully with the specific catalytic elements added to the aluminous substances serving as supports. Thus, for example, recommended stabilizers such as silica, magnesia
Another way to avoid the progressive transformation -of active aluminas by loss of water at high temperatures comprises adding various oxides thereto which act as stabilizers. With this aim, the most frequently recommended oxides are those of the alkaline and alkaline earth metals, oxides of the metals of Group III A of the periodic table, oxides of thorium and oxides of silicon. However, the instructions given in the past are frequently of too general a nature to permit preparation, wi*h certainty, of suffi-ciently interesting results for industrial exploitation,and, furthermore, certain recommended additives can inter-fere harmfully with the specific catalytic elements added to the aluminous substances serving as supports. Thus, for example, recommended stabilizers such as silica, magnesia
3 and the oxides of the rare earth metals are each specific -.
106042~
to this or that active alumina, the various oxides of ~he rare earth metals do not have identical actions and the oxides of the alkali metals, likewise recommended as stabilizers, cannot be introduced into the supports of cer-tain catalysts since they act then as catalytic poisons,which is frequently the case with the above-mentioned silica.
It has been sought to improve the alumina sub-stances, intended for use as catalyst supports, obtained by agglomeration of active alumina particles (in particular, those prepared from the partial dehydration of hydrargillite and alumina gels in hot gas currents) and have found that such ~ubstances when autoclaved, and in particular auto-claved in the presence ofacids, are stabilized in a very effective manner up to a temperature reaching 1200C by the -~
oxides of certain of the rare earth metals which are those of lanthanum, neodymium and praseodymium, and by oxides of thorium. Moreover, it is preferable to avoid, as far as possible, the presence of compounds of the alkali metals and especially that of sodium which frequently has a harmful - effect upon the catalytic properties, as indicated above.
Such substances occasionally posses not only a specific surface which decreases relatively less rapidly with temperature,-but also a greater solidity for a greater porous volume. In industrial practice, while the substances obtained from hydrargillite already possess a very interesting set of characteristics, it is sometimes necessary to obtain substances which are lighter and yet are sufficiently resis-tant. Alumina geLs facilitate the preparation of such sub-3 stances which can further display higher specific surfaces at high temperature than those obtained from hydrargillite. It should benoted, however, that as a result of the great porous volume of the alumina-basecl substances obtained from gels, one cannot obtain such high crushing resistances as those of the more dense substances obtained from active aluminas prepared from the dehydration of hydrargillite; the attrition resistances obtained are, however, high and unexpectedly exhibit values at least equal to those obtained for substances derived from hydrargillite. That is of great interest for all applications where vibrations of the apparatuses are inevitable.
The present invention provides a process for preparing an alumina-based substance stabilized to a calcination temperature of approximately 1200C, comprising calcining at a temperature up to approximately 1200C a mixture comprising autoclaved alumina ant 1 to 15% by weight of at least one additive selected from the group consisting of the oxides of lanthanum, nsodymium praseodymium and thorium, said autoclaved alumina having been produced by partial dehydration of hydrargillite or an alumina gel to produce activated alumina, then autoclaving the activated alumina to form said alumina, The present invention also pertains to an alumina-based substance stabilized to calcination temperatures up to 1200C comprising 99 to 85% by weight alumina which has been calcined up to 1200C and 1 to 15% by weight of at least one additive selected from the group consisting of oxides of lan-thanum, neodymium, praseodymium, and thorium said additive or a precursor thereof having been calcined with said aluminum, said substance having a gIain density of from about 1.20 to 1.25; a surface area of from about 20 to 30 m2/g and an attrition resistance of at least about 98%.
,l ~ ~ -5-The proportions to be utilized of the oxides under consideration are between 1% and 15% by weight of the quantity of alumina of these substan-ces, and, more particularly~ between 2% and 7%; it should be noted that these proportions are quite clearly lower than those frequently utilized in certain catalysts where oxides of the rare earth metals play a catalytic part, par-ticularly at temperatures at which the stabilizing effect does not have to intervene.
The alumina based substances according to the invention can be obtained in different ways. For example, one can add the oxides or the oxide precursors of the metals enumerated above by mixture or impregnation of alumina hydrates before their activation by dehydration, their agglomeration and the autoclaving of the substances obtained; it is likewise possible to add these same oxides or their precursors to active alumina powders obtained by dehydration of alumina hydrates, and then to effect the agglomeration of these powders, and then employ the autoclave treatment of the substances obtained. It is also possible to add the i~ -Sa-~..
precursors of these oYides by impregnation to the substances obtained by agglomeration of active alumina powder, and then to treat these substances in the autoclave. Finally, and in preferred manner, it is possible to add the precursors of the oxides under consideration by impregnation after the treatment of the alumina substances in the autoclave, and more preferably, after a reactivation following auto-clave treatment however, in the case where the alumina substances are derived from gels, it is further possible to operate by coprecipitation of solutions containing aluminum salts and salts of the rare earth metals at the -~
same time, as precursors of the alumina and of the various added oxides; this latter process provides very great homogeneity of the finished products.
.~
'~ According to the selected manner of addition of the considered oxides to the alumina substances, one can be led to additional drying and calcination operations;
these procedures are well known and need not be described in detail.
In any case, the alumina-based substances thus obtained are then dried and calcined at the selected tem-perature which can reach approximately 1200C, as indicated previously. To illustrate the present invention, various examples are given below concerning substances obtained from hydrargillite and from alumina gel, along with compara-tive examples showing that the unautoclaved substances are not improved b~ the oxides which are effective ~n the autoclaved substances, and that the oxides of certain other rare earth metals have Iittle action.
3 For the examples in which the substances are obtained from hydrargillite, as initial product one utilizes alumina balls of diameters of between 2.5 and 4 mm, obtained by agglomeration in a rotating granulator of hydrargillite prepared in accordance with the Bayer process after partial dehydration in a current of hot gases: these balls are washed to reduce their Na2O content to less than 0.2%, then calcined at 600C for the purpose of activation. These balls have a specific surface of 250 sq.m./g., a grain density of 1.22, a grain-by-grain crushing resistance of 10 kg (average), and an attrition resistance measured by the microgrinder of 97.5%; hereinafter these balls are called support A. A portion of these balls is subjected to an autoclave treatment in the presence of acetic acid,then reactivated at 600C. The support thus obtained, called support B, has a specific surface of 90 sq.m./g., a grain density of 1.20, a grain-by-grain crushing resistance of 11 kg and an attrition resistance of 99.7%. These supports A
and B and the different products obtained from these supports by various additions of oxides are then calcined at 120~C
for four hours; the same characteristics as those indicated for the supports A and B are measured on all these samples.
For the examples concerning the substances obtained from~alumina gelc, the initial product called support M is in the form of balls of diameter between 2.5 and,4 mm ob-tained by agglomeration in a rotating granulator of an alu-mina powdex obtained by partial dehydration in a hot gas current of a washed and dried alumina gel obtained by pre-, cipitation of sodium aluminate with nitric acid at a pHbetween 9 and 10. This washed and dried gel, examined by 3~ X-rays, proves to be a mixtuxe of monohydroxides of the pseudoboehmite type and trihydroxides of the bayerite and hydrargillite type. After agglomeration, the balls are ripened in water vapor atmosphe~es, then dried and calcined at 500C. After calcination at 600OC for four hours, support M has a grain density of 0.76, a specific surface of 2~0 sq.m./g., a crushing resistance of 7.4 kg and an attrition resistance of 99.~/O. This support and the differ-ent products obtained by adding oxides of praseodymium and didymium thereto are calcined at 1000 and 1200C for 4 -hours. The same characteristics as those indicated previously are measured on these various samples.
Different fractions of the support B are impreg-nated with solutions of the nitrates of lanthanum, neo-dymium, praseodymium and thorium in concentrations such that after calcination, the supports contain 4% of the various oxides in relation to the alumina.
EX~MPLE 2 This example is a comparative example and concerns substances ob~ ined from the supports B to which, in a manner analogous to that described in Example 1, in relation to the alumina there are added 4% by weight o~ the oxides of samarium, gadolinium and yttrium, which exhibit little effect.
25 ~ EXAMPLE 3 This example concerns substances containing dif-ferent proportions of the oxides of lanthanum and neodymium;
these substances are obtained from supports B in the manner indicated in Example 1.
This example concerns substances containing additions o 4% by weight in relation to the alumina of the oxides of lanthanum and neodymium; they are obtained by the calcination of supports B impregnated by solutions o~
metal chlorides.
This comparative example concerns substances obtained rom the supports A to which there are added 4%
by weight, in relation to the alumina, of neodymium oxide by impregnation with the corresponding nitrate.
The various results are combined in the ollowing Table I in which there likewise appear the results relating to supports ~ and B calcined at 1200C, serving as control.
~5 ~ .
.
10604Z~
TABI,E I
. _ Supports by wéightMetal Grain Speci~icl Mean Attrition or of oxides of thedensity surface - resis- resis-Examples in rela-oxide sqOm./g. tance tance tion to to %
alumina crush-ing kg _ _ Support A cal- 0 _ 1.45 10 3 70 cined 1200C :
Suppo~t B cal- 0 _ 1.4 6 10 97 cined 1200C :
. _ . ._ .
1 4 ~a 1.25 30 15 99.3
106042~
to this or that active alumina, the various oxides of ~he rare earth metals do not have identical actions and the oxides of the alkali metals, likewise recommended as stabilizers, cannot be introduced into the supports of cer-tain catalysts since they act then as catalytic poisons,which is frequently the case with the above-mentioned silica.
It has been sought to improve the alumina sub-stances, intended for use as catalyst supports, obtained by agglomeration of active alumina particles (in particular, those prepared from the partial dehydration of hydrargillite and alumina gels in hot gas currents) and have found that such ~ubstances when autoclaved, and in particular auto-claved in the presence ofacids, are stabilized in a very effective manner up to a temperature reaching 1200C by the -~
oxides of certain of the rare earth metals which are those of lanthanum, neodymium and praseodymium, and by oxides of thorium. Moreover, it is preferable to avoid, as far as possible, the presence of compounds of the alkali metals and especially that of sodium which frequently has a harmful - effect upon the catalytic properties, as indicated above.
Such substances occasionally posses not only a specific surface which decreases relatively less rapidly with temperature,-but also a greater solidity for a greater porous volume. In industrial practice, while the substances obtained from hydrargillite already possess a very interesting set of characteristics, it is sometimes necessary to obtain substances which are lighter and yet are sufficiently resis-tant. Alumina geLs facilitate the preparation of such sub-3 stances which can further display higher specific surfaces at high temperature than those obtained from hydrargillite. It should benoted, however, that as a result of the great porous volume of the alumina-basecl substances obtained from gels, one cannot obtain such high crushing resistances as those of the more dense substances obtained from active aluminas prepared from the dehydration of hydrargillite; the attrition resistances obtained are, however, high and unexpectedly exhibit values at least equal to those obtained for substances derived from hydrargillite. That is of great interest for all applications where vibrations of the apparatuses are inevitable.
The present invention provides a process for preparing an alumina-based substance stabilized to a calcination temperature of approximately 1200C, comprising calcining at a temperature up to approximately 1200C a mixture comprising autoclaved alumina ant 1 to 15% by weight of at least one additive selected from the group consisting of the oxides of lanthanum, nsodymium praseodymium and thorium, said autoclaved alumina having been produced by partial dehydration of hydrargillite or an alumina gel to produce activated alumina, then autoclaving the activated alumina to form said alumina, The present invention also pertains to an alumina-based substance stabilized to calcination temperatures up to 1200C comprising 99 to 85% by weight alumina which has been calcined up to 1200C and 1 to 15% by weight of at least one additive selected from the group consisting of oxides of lan-thanum, neodymium, praseodymium, and thorium said additive or a precursor thereof having been calcined with said aluminum, said substance having a gIain density of from about 1.20 to 1.25; a surface area of from about 20 to 30 m2/g and an attrition resistance of at least about 98%.
,l ~ ~ -5-The proportions to be utilized of the oxides under consideration are between 1% and 15% by weight of the quantity of alumina of these substan-ces, and, more particularly~ between 2% and 7%; it should be noted that these proportions are quite clearly lower than those frequently utilized in certain catalysts where oxides of the rare earth metals play a catalytic part, par-ticularly at temperatures at which the stabilizing effect does not have to intervene.
The alumina based substances according to the invention can be obtained in different ways. For example, one can add the oxides or the oxide precursors of the metals enumerated above by mixture or impregnation of alumina hydrates before their activation by dehydration, their agglomeration and the autoclaving of the substances obtained; it is likewise possible to add these same oxides or their precursors to active alumina powders obtained by dehydration of alumina hydrates, and then to effect the agglomeration of these powders, and then employ the autoclave treatment of the substances obtained. It is also possible to add the i~ -Sa-~..
precursors of these oYides by impregnation to the substances obtained by agglomeration of active alumina powder, and then to treat these substances in the autoclave. Finally, and in preferred manner, it is possible to add the precursors of the oxides under consideration by impregnation after the treatment of the alumina substances in the autoclave, and more preferably, after a reactivation following auto-clave treatment however, in the case where the alumina substances are derived from gels, it is further possible to operate by coprecipitation of solutions containing aluminum salts and salts of the rare earth metals at the -~
same time, as precursors of the alumina and of the various added oxides; this latter process provides very great homogeneity of the finished products.
.~
'~ According to the selected manner of addition of the considered oxides to the alumina substances, one can be led to additional drying and calcination operations;
these procedures are well known and need not be described in detail.
In any case, the alumina-based substances thus obtained are then dried and calcined at the selected tem-perature which can reach approximately 1200C, as indicated previously. To illustrate the present invention, various examples are given below concerning substances obtained from hydrargillite and from alumina gel, along with compara-tive examples showing that the unautoclaved substances are not improved b~ the oxides which are effective ~n the autoclaved substances, and that the oxides of certain other rare earth metals have Iittle action.
3 For the examples in which the substances are obtained from hydrargillite, as initial product one utilizes alumina balls of diameters of between 2.5 and 4 mm, obtained by agglomeration in a rotating granulator of hydrargillite prepared in accordance with the Bayer process after partial dehydration in a current of hot gases: these balls are washed to reduce their Na2O content to less than 0.2%, then calcined at 600C for the purpose of activation. These balls have a specific surface of 250 sq.m./g., a grain density of 1.22, a grain-by-grain crushing resistance of 10 kg (average), and an attrition resistance measured by the microgrinder of 97.5%; hereinafter these balls are called support A. A portion of these balls is subjected to an autoclave treatment in the presence of acetic acid,then reactivated at 600C. The support thus obtained, called support B, has a specific surface of 90 sq.m./g., a grain density of 1.20, a grain-by-grain crushing resistance of 11 kg and an attrition resistance of 99.7%. These supports A
and B and the different products obtained from these supports by various additions of oxides are then calcined at 120~C
for four hours; the same characteristics as those indicated for the supports A and B are measured on all these samples.
For the examples concerning the substances obtained from~alumina gelc, the initial product called support M is in the form of balls of diameter between 2.5 and,4 mm ob-tained by agglomeration in a rotating granulator of an alu-mina powdex obtained by partial dehydration in a hot gas current of a washed and dried alumina gel obtained by pre-, cipitation of sodium aluminate with nitric acid at a pHbetween 9 and 10. This washed and dried gel, examined by 3~ X-rays, proves to be a mixtuxe of monohydroxides of the pseudoboehmite type and trihydroxides of the bayerite and hydrargillite type. After agglomeration, the balls are ripened in water vapor atmosphe~es, then dried and calcined at 500C. After calcination at 600OC for four hours, support M has a grain density of 0.76, a specific surface of 2~0 sq.m./g., a crushing resistance of 7.4 kg and an attrition resistance of 99.~/O. This support and the differ-ent products obtained by adding oxides of praseodymium and didymium thereto are calcined at 1000 and 1200C for 4 -hours. The same characteristics as those indicated previously are measured on these various samples.
Different fractions of the support B are impreg-nated with solutions of the nitrates of lanthanum, neo-dymium, praseodymium and thorium in concentrations such that after calcination, the supports contain 4% of the various oxides in relation to the alumina.
EX~MPLE 2 This example is a comparative example and concerns substances ob~ ined from the supports B to which, in a manner analogous to that described in Example 1, in relation to the alumina there are added 4% by weight o~ the oxides of samarium, gadolinium and yttrium, which exhibit little effect.
25 ~ EXAMPLE 3 This example concerns substances containing dif-ferent proportions of the oxides of lanthanum and neodymium;
these substances are obtained from supports B in the manner indicated in Example 1.
This example concerns substances containing additions o 4% by weight in relation to the alumina of the oxides of lanthanum and neodymium; they are obtained by the calcination of supports B impregnated by solutions o~
metal chlorides.
This comparative example concerns substances obtained rom the supports A to which there are added 4%
by weight, in relation to the alumina, of neodymium oxide by impregnation with the corresponding nitrate.
The various results are combined in the ollowing Table I in which there likewise appear the results relating to supports ~ and B calcined at 1200C, serving as control.
~5 ~ .
.
10604Z~
TABI,E I
. _ Supports by wéightMetal Grain Speci~icl Mean Attrition or of oxides of thedensity surface - resis- resis-Examples in rela-oxide sqOm./g. tance tance tion to to %
alumina crush-ing kg _ _ Support A cal- 0 _ 1.45 10 3 70 cined 1200C :
Suppo~t B cal- 0 _ 1.4 6 10 97 cined 1200C :
. _ . ._ .
1 4 ~a 1.25 30 15 99.3
4 Nd 1O25 27 14 99.3 Support 4 Pr 1.25 28 14 99 B 4 Th 1.25 28 15 99 (ex ni- .
trates) .
... _ ._ 2 4 Sm _ 18 11 97 4 Gd _ 15 10 97 Support 4 Y _ 13 11 97 B teraXtensi) .. __ .__ 3 2 La 1.25 24 13 98.2 La 1.25 17 15 . 99.2 Support 2 Nd 1.25 15 14 98.3 B 10 Nd 1.25 22 13 99 (ex ni-. trates) .
... _ .
4 4 La 1.25 28 . 14 99 4 Nd 1.25 21 14 99 Support . (ex B chlo-. rides) .
.. . ._ 4 Nd 1.45 14 5 75 Support (ex ni trate) . _ .
.
This ~rable permits various comparisons: Firstly, the particular effect of certain oxides is clearly shown by comparison of Examples 1 and 2 since the oxides of samarium, gadolinium and yttrium have practically no effect upon the mechanical resistance although they permit a certain stabilization of the specific surface, whereas the oxides of lanthanum, neodymium, praseodymium and thorium act simultaneously upon the values of the mechanical resistance and specific surface. Putting the results of Example 3 together with the results concerning lanthanum and neodymium from Example 1 shows that the quantity of added oxides can be quite small since the addition of 2% of lanthanum or neodymium has a very great stabilization effect, and that this added quantity diminishes the value of the specific surface beyond a certain value. Comparison of Examples 1 and 5 shows the necessity of effecting autoclaving since neodymium, the efficacity of which is demonstrated, added to support A, somewhat slightly stabilizes the specific surface but only very insufficiently increases the mechanical resistance. Finally, Example 4 shows that the origin of the oxides is immaterial. In general, it should be noted that the grain density is stabilized at a value clearly below that of the supports without addition of oxides, which thus corresponds to a greater porosity which is often necessary in catalyst supports.
This example is given by way of com~ rison; support M is impregnated with a solution of didymium nitrate which is a mixture of the nitrates of praseodymium and neodymium, 3 the quantity of this solution being such that it exactly fills the porous volume of the support and its concentratiOn being such that after drying and calcination the oxides of praseodymium and neodymium represent 4% of the weight o~
the alumina.
This same support M impregnated with 5% of its weight of acetic acid is autoclaved for 6 hours at a pressure of 12 bars absolute at about 185C in an atmos-phere of water vapor, then calcined at 500C for the purpose of reactivation; it is then impregnated as indicated in Example 6, dried and calcined.
Support M is impregnated by an acetic solution of didymium acetate of such concentration and in such quantity that the introduced quantity of acetic anions is 10% by weight of the anhydrous support and that the quantity of didymium acetate corresponds, expressed as the oxide, to 4% of the weight of this support. The support thus impreg-nated is autoclaved as indicated in Example 7, then dried and calcined.
The following Table II brings together the results obtained and those concerning the calcined support M serving as control; moreover, in this table there are shown the results concerning support B of Table I with 4% of neodymium 25~ oxide mentioned in Example 4, the calcinations being effected at lO00 and 1200~C.
TABLE II
Grain density Specific surface Mean crushing Attrition Examples resistance in resistance after calcin- sq.m./g. a~ter kg after in % after calcination calcination at calcination ation at at at . ~ .
Cupepdortt 1000C 0.861.11 70 6 3.1 0.5 99.7 86 . .. __ . .
6 0.88 1 105 25 5 4.7 99 98.0 ' 7 0.790.85 75 30 4 3.5 99.9 99.7 . . __ ._ 8 0.790.86 80 32 4.5 4 g9.9 99.8 ', Sup iort wieght 1.201~25 50 21 14 14 99 99 of neo-oxid- _ _ _ The results of this table show clearly that the improvement effected by the presence of the oxides of praseo-dymium and neodymium (Example 6) in comparison with the results obtained for the control is increased by autoclaving (Examples 7 and 8); these results are to be compared with the characteristics given previously of the support M cal-cined at 600C, particularly as regards the slight increase of the grain density of the substances of Examples 7 and 8 which are in accordance with the invention. Finally, the comparison of the results given by the products deriving from an alumina gel with those given by the product deriving ... .
from hydrargillite shows that the products deriving from gels are clearly lighter and have a higher specific surface.
: ' ~:
:
.
~ 3~ `
trates) .
... _ ._ 2 4 Sm _ 18 11 97 4 Gd _ 15 10 97 Support 4 Y _ 13 11 97 B teraXtensi) .. __ .__ 3 2 La 1.25 24 13 98.2 La 1.25 17 15 . 99.2 Support 2 Nd 1.25 15 14 98.3 B 10 Nd 1.25 22 13 99 (ex ni-. trates) .
... _ .
4 4 La 1.25 28 . 14 99 4 Nd 1.25 21 14 99 Support . (ex B chlo-. rides) .
.. . ._ 4 Nd 1.45 14 5 75 Support (ex ni trate) . _ .
.
This ~rable permits various comparisons: Firstly, the particular effect of certain oxides is clearly shown by comparison of Examples 1 and 2 since the oxides of samarium, gadolinium and yttrium have practically no effect upon the mechanical resistance although they permit a certain stabilization of the specific surface, whereas the oxides of lanthanum, neodymium, praseodymium and thorium act simultaneously upon the values of the mechanical resistance and specific surface. Putting the results of Example 3 together with the results concerning lanthanum and neodymium from Example 1 shows that the quantity of added oxides can be quite small since the addition of 2% of lanthanum or neodymium has a very great stabilization effect, and that this added quantity diminishes the value of the specific surface beyond a certain value. Comparison of Examples 1 and 5 shows the necessity of effecting autoclaving since neodymium, the efficacity of which is demonstrated, added to support A, somewhat slightly stabilizes the specific surface but only very insufficiently increases the mechanical resistance. Finally, Example 4 shows that the origin of the oxides is immaterial. In general, it should be noted that the grain density is stabilized at a value clearly below that of the supports without addition of oxides, which thus corresponds to a greater porosity which is often necessary in catalyst supports.
This example is given by way of com~ rison; support M is impregnated with a solution of didymium nitrate which is a mixture of the nitrates of praseodymium and neodymium, 3 the quantity of this solution being such that it exactly fills the porous volume of the support and its concentratiOn being such that after drying and calcination the oxides of praseodymium and neodymium represent 4% of the weight o~
the alumina.
This same support M impregnated with 5% of its weight of acetic acid is autoclaved for 6 hours at a pressure of 12 bars absolute at about 185C in an atmos-phere of water vapor, then calcined at 500C for the purpose of reactivation; it is then impregnated as indicated in Example 6, dried and calcined.
Support M is impregnated by an acetic solution of didymium acetate of such concentration and in such quantity that the introduced quantity of acetic anions is 10% by weight of the anhydrous support and that the quantity of didymium acetate corresponds, expressed as the oxide, to 4% of the weight of this support. The support thus impreg-nated is autoclaved as indicated in Example 7, then dried and calcined.
The following Table II brings together the results obtained and those concerning the calcined support M serving as control; moreover, in this table there are shown the results concerning support B of Table I with 4% of neodymium 25~ oxide mentioned in Example 4, the calcinations being effected at lO00 and 1200~C.
TABLE II
Grain density Specific surface Mean crushing Attrition Examples resistance in resistance after calcin- sq.m./g. a~ter kg after in % after calcination calcination at calcination ation at at at . ~ .
Cupepdortt 1000C 0.861.11 70 6 3.1 0.5 99.7 86 . .. __ . .
6 0.88 1 105 25 5 4.7 99 98.0 ' 7 0.790.85 75 30 4 3.5 99.9 99.7 . . __ ._ 8 0.790.86 80 32 4.5 4 g9.9 99.8 ', Sup iort wieght 1.201~25 50 21 14 14 99 99 of neo-oxid- _ _ _ The results of this table show clearly that the improvement effected by the presence of the oxides of praseo-dymium and neodymium (Example 6) in comparison with the results obtained for the control is increased by autoclaving (Examples 7 and 8); these results are to be compared with the characteristics given previously of the support M cal-cined at 600C, particularly as regards the slight increase of the grain density of the substances of Examples 7 and 8 which are in accordance with the invention. Finally, the comparison of the results given by the products deriving from an alumina gel with those given by the product deriving ... .
from hydrargillite shows that the products deriving from gels are clearly lighter and have a higher specific surface.
: ' ~:
:
.
~ 3~ `
Claims (14)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A process for preparing an alumina-based substance stabilized to a calcination temperature of approximately 1200°C, comprising calcining at a temperature up to approximately 1200°C a mixture comprising autoclaved alumina and 1 to 15% by weight of at least one additive selected from the group consisting of the oxides of lanthanum, neodymium praseodymium and thorium, said autoclaved alumina having been produced by partial dehydration of hydrargillite or an alumina gel to produce activated alumina, then auto-claving the activated alumina to form said alumina.
2. A process according to claim 1 wherein the autoclaving is effected in the presence of acid.
3. A process according to claim 1 wherein the proportion of oxides is between 2 and 7% by weight of the alumina.
4. A process according to claim 1 wherein the alumina is derived from hydrargillite.
5. A process according to claim 1 wherein the alumina is derived from alumina gels.
6. A process according to claim 1 wherein the alumina is derived from hydrargillite or alumina gels partially dehydrated in hot gas currents.
7. A process according to claim 6 wherein precursors of the oxides or oxide are added to the partially dehydrated alumina and its agglomeration is effected.
8. A process according to claim 1 wherein previously autoclaved alu-mina substances are impregnated by solutions of oxide precursor compounds, then calcined.
9. A process according to claim 8 wherein previously autoclaved alumina substances are further activated be-fore impregnation.
10. A process according to claim 1 wherein the alumina is impregnated by solutions of oxide precursor compounds before autoclave treatment.
11. A process according to claim 1 wherein precursors of the oxide or oxides are added to the hydrarqillile before its transformation into active alumina and agglomeration of active alumina is effected in the form of substances which are then autoclave treated.
12. A process according to claim 5 wherein the alumina based substance is by coprecipitation of aluminum salts and salts of lanthanum, neodymium, praseodymium or thorium.
13. A process according to claim 1 wherein the alumina based substance is substantially free of alkali metal compounds.
14. An alumina-based substance stabilized to calcination temperatures up to 1200°C comprising 99 to 85% by weight alumina which has been calcined up to 1200°C and 1 to 15%
by weight of at least one additive selected from the group consisting of oxides of lanthanum, neodymium, praseo-dymium, and thorium said additive or a precursor thereof having been calcined with said aluminum, said substance having a grain density of from about 1.20 to 1.25; a sur-face area of from about 20 to 30 m2/g and an attrition resistance of at least about 98%.
by weight of at least one additive selected from the group consisting of oxides of lanthanum, neodymium, praseo-dymium, and thorium said additive or a precursor thereof having been calcined with said aluminum, said substance having a grain density of from about 1.20 to 1.25; a sur-face area of from about 20 to 30 m2/g and an attrition resistance of at least about 98%.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7400803A FR2257335A1 (en) | 1974-01-10 | 1974-01-10 | Refractory alumina agglomerates for use as catalyst carriers - contg. metal oxide additives for improved heat stability |
| FR7437892A FR2290950A2 (en) | 1974-11-18 | 1974-11-18 | Refractory alumina agglomerates for use as catalyst carriers - contg. metal oxide additives for improved heat stability |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1060424A true CA1060424A (en) | 1979-08-14 |
Family
ID=26218123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA217,700A Expired CA1060424A (en) | 1974-01-10 | 1975-01-10 | Alumina-based bodies obtained by agglomeration which are resistant to elevated temperatures |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS5651152B2 (en) |
| CA (1) | CA1060424A (en) |
| CH (1) | CH605465A5 (en) |
| ES (1) | ES433643A1 (en) |
| GB (1) | GB1488281A (en) |
| IT (1) | IT1026273B (en) |
| LU (1) | LU71607A1 (en) |
| NL (1) | NL190227C (en) |
| SE (1) | SE417912B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3974256A (en) * | 1974-05-07 | 1976-08-10 | Exxon Research And Engineering Company | Sulfide removal process |
| JPS6031747U (en) * | 1983-08-08 | 1985-03-04 | パイオニア株式会社 | Reel motor drive control circuit |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1386364A (en) * | 1963-12-02 | 1965-01-22 | Pechiney Saint Gobain | Porous active alumina of great mechanical strength |
| FR1449904A (en) * | 1965-07-09 | 1966-05-06 | Pechiney Saint Gobain | High mechanical strength active alumina agglomerates |
| US3899444A (en) * | 1972-02-07 | 1975-08-12 | Ethyl Corp | Exhaust gas catalyst support |
-
1975
- 1975-01-08 ES ES433643A patent/ES433643A1/en not_active Expired
- 1975-01-08 NL NLAANVRAGE7500198,A patent/NL190227C/en not_active IP Right Cessation
- 1975-01-09 GB GB960/75A patent/GB1488281A/en not_active Expired
- 1975-01-09 LU LU71607A patent/LU71607A1/xx unknown
- 1975-01-09 CH CH19375A patent/CH605465A5/xx not_active IP Right Cessation
- 1975-01-09 SE SE7500226A patent/SE417912B/en not_active IP Right Cessation
- 1975-01-09 IT IT47578/75A patent/IT1026273B/en active
- 1975-01-10 CA CA217,700A patent/CA1060424A/en not_active Expired
- 1975-01-10 JP JP550875A patent/JPS5651152B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1488281A (en) | 1977-10-12 |
| NL7500198A (en) | 1975-07-14 |
| SE417912B (en) | 1981-04-27 |
| ES433643A1 (en) | 1977-02-16 |
| DE2500548A1 (en) | 1975-07-17 |
| NL190227C (en) | 1993-12-16 |
| CH605465A5 (en) | 1978-09-29 |
| JPS5651152B2 (en) | 1981-12-03 |
| JPS50116504A (en) | 1975-09-11 |
| NL190227B (en) | 1993-07-16 |
| LU71607A1 (en) | 1975-12-09 |
| SE7500226L (en) | 1975-07-11 |
| DE2500548B2 (en) | 1977-06-23 |
| IT1026273B (en) | 1978-09-20 |
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