Chromium-aluminum-phosphorus-oxide molecular sieve compositions

Abstract

Molecular sieve compositions having three-dimensional microporous framework structures of CrO.sub.2, AlO.sub.2 and PO.sub.2 tetrahedral oxide units are disclosed. These molecular sieves have an empirical chemical composition on an anhydrous basis expressed by the formula:mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 ; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides. Their use as adsorbents, catalysts, etc. is also disclosed.

Description

FIELD OF THE INVENTION

The instant invention relates to a novel class of crystalline microporous molecular sieves and to the method of their preparation. The invention relates to novel chromium-aluminum-phosphorus-oxide molecular sieves containing framework tetrahedral oxide units of chromium, aluminum and phosphorus. These compositions may be prepared hydrothermally from gels containing reactive compounds of chromium, aluminum and phosphorus capable of forming framework tetrahedral oxides, and preferably at least one organic templating agent which functions in part to determine the course of the crystallization mechanism and the structure of the crystalline product.

BACKGROUND OF THE INVENTION

Molecular sieves of the crystalline aluminosilicate zeolite type are well known in the art and now comprise over 150 species of both naturally occurring and synthetic compositions. In general the crystalline zeolites are formed from corner-sharing AlO.sub.2 and SiO.sub.2 tetrahedra and are characterized by having pore openings of uniform dimensions, having a significant ion-exchange capacity and being capable of reversibly desorbing an adsorbed phase which is dispersed throughout the internal voids of the crystal without displacing any atoms which make up the permanent crystal structure.

Other crystalline microporous compositions which are not zeolitic, i.e. do not contain AlO.sub.2 tetrahedra as essential framework constituents, but which exhibit the ion-exchange and/or adsorption characteristics of the zeolites are also known. Metal organosilicates which are said to possess ion-exchange properties, have uniform pores and are capable of reversibly adsorbing molecules having molecular diameters of about 6 .ANG. or less, are reported in U.S. Pat. No. 3,941,871 issued Mar. 2, 1976 to Dwyer et al. A pure silica polymorph, silicalite, having molecular sieving properties and a neutral framework containing neither cations nor cation sites is disclosed in U.S. Pat. No. 4,061,724 issued Dec. 6, 1977 to R. W. Grose et al.

A recently reported class of microporous compositions and the first framework oxide molecular sieves synthesized without silica, are the crystalline aluminophosphate compositions disclosed in U.S. Pat. No. 4,310,440 issued Jan. 12, 1982 to Wilson et al. These materials are fomred from AlO.sub.2 and PO.sub.2 tetrahedra and have electrovalently neutral frameworks as in the case of silica polymorphs. Unlike the silica molecular sieve, silicalite, which is hydrophobic due to the absence of extra-structural cations, the aluminophosphate molecular sieves are moderately hydrophilic, apparently due to the difference in electronegativity between aluminum and phosphorus. Their intracrystalline pore volumes and pore diameters are comparable to those known for zeolites and silica molecular sieves.

In U.S. Pat. No. 4,440,871 there is described a novel class of silicon-substituted aluminophosphates which are both microporous and crystalline. The materials have a three dimensional crystal framework of PO.sub.2.sup.+, AlO.sub.2.sup.- and SiO.sub.2 tetrahedral units and, exclusive of any alkali metal or calcium which may optionally be present, an as-synthesized empirical chemical composition on an anhydrous basis of:

mR:(Si.sub.x Al.sub.y P.sub.z)O.sub.2 wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the moles of "R" present per mole of (Si.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to 0.3, the maximum value in each case depending upon the molecular dimensions of the templating agent and the available void volume of the pore system of the particular silicoaluminophosphate species involved; and "x", "y", and "z" represent the mole factions of silicon, aluminum and phosphorus, respectively, present as tetrahedral oxides. The minimum value for each of "x", "y", and "z" is 0.01 and preferably 0.02. The maximum value for "x" is 0.98; for "y" is 0.60; and for "z" is 0.52. These silicoaluminophosphates exhibit several physical and chemical properties which are characteristic of aluminosilicate zeolites and aluminophosphates.

In U.S. Pat. No. 4,500,651, there is described a novel class of titanium-containing molecular sieves whose chemical composition in the as-synthesized and anhydrous form is represented by the unit empirical formula:

mR:(Ti.sub.x Al.sub.y P.sub.z)O.sub.2 wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the moles of "R" present per mole of (Ti.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of between zero and about 5.0; and "x", "y" and "z" represent the mole fractions of titanium, aluminum and phosphorus, respectively, present as tetrahedral oxides.

In U.S. Pat. No. 4,567,029, there is described a novel class of crystalline metal aluminophosphates having three-dimensional microporous framework structures of MO.sub.2, AlO.sub.2 and PO.sub.2 tetrahedral units and having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(M.sub.x Al.sub.y P.sub.z)O.sub.2 wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the moles of "R" present per mole of (M.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to 0.3; "M" represents at least one metal of the group magnesium, manganese, zinc and cobalt; "x", "y", and "z" represent the mole fractions of the metal "M", aluminum and phosphorus, respectively, present as tetrahedral oxides.

In U.S. Pat. No. 4,544,143, there is described a novel class of crystalline ferroaluminophosphates having a three-dimensional microporous framework structure of FeO.sub.2, AlO.sub.2 and PO.sub.2 tetrahedral units and having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Fe.sub.x Al.sub.y P.sub.z)O.sub.2 wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the moles of "R" present per mole of (Fe.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to 0.3; and "x", "y" and "z" represent the mole fractions of the iron, aluminum and phosphorus, respectively, present as tetrahedral oxides.

The instant invention relates to new molecular sieve compositions having framework tetrahedral units of CrO.sub.2.sup.n, AlO.sub.2.sup.- and PO.sub.2.sup.+ where "n" is -1, 0 or +1.

DESCRIPTION OF THE FIGURES

FIG. 1 is a ternary diagram wherein parameters relating to the instant compositions are set forth as mole fractions for when "n" equals -1 or +1, as hereinafter discussed.

FIG. 2 is a ternary diagram wherein parameters relating to the instant compositions are set forth as mole fractions for when "n" equals zero, as hereinafter discussed.

FIG. 3 is a ternary diagram wherein parameters relating to preferred compositions are set forth as mole fractions.

FIG. 4 is a ternary diagram wherein parameters relating to preferred compositions are set forth as mole fractions.

FIG. 5 is a ternary diagram wherein parameters relating to preferred compositions are set forth as mole fractions.

FIG. 6 is a ternary diagram wherein parameters relating to the reaction mixtures employed in the preparation of the compositions of this invention are set forth as mole fractions.

SUMMARY OF THE INVENTION

The instant invention relates to a new class of chromium-aluminum-phosphorus-oxide molecular sieves having a crystal framework structure of CrO.sub.2.sup.n, AlO.sub.2.sup.- and PO.sub.2.sup.+ tetrahedral oxide units where "n" is -1, 0 or +1. These new molecular sieves exhibit ion-exchange, adsorption and catalytic properties and, accordingly, find wide use as adsorbents and catalysts. The members of this novel class of compositions have crystal framework structures of CrO.sub.2.sup.n, AlO.sub.2.sup.- and PO.sub.2.sup.+ tetrahedral units and have an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2 wherein "R"represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides. These molecular sieve compositions comprise crystalline molecular sieves having a three-dimensional microporous framework structure of CrO.sub.2.sup.n, AlO.sub.2.sup.- and PO.sub.2.sup.+ tetrahedral units where "n" is -1, 0 or +1.

The molecular sieves of the instant invention will be generally referred to by the acronym "CAPO" to designate the framework of CrO.sub.2.sup.n, AlO.sub.2.sup.- and PO.sub.2.sup.+ tetrahedral units. Actual class members will be identified by denominating the various structural species which make up the CAPO class by assigning a number and, accordingly, are identified as "CAPO-i" wherein "i" is an integer. The given species designation is not intended to denote a similarity in structure to any other species denominated by a numbering system.

DETAILED DESCRIPTION OF THE INVENTION

The instant invention relates to a new class of chromium-aluminum-phosphorus-oxide molecular sieves comprising a crystal framework structure of CrO.sub.2.sup.n, AlO.sub.2.sup.- and PO.sub.2.sup.+ tetrahedral oxide units, where "n" is -1, 0 or +1. These new molecular sieves exhibit ion-exchange, adsorption and catalytic properties and, accordingly, find wide use as adsorbents and catalysts.

The CAPO molecular sieves of the instant invention comprise three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2.sup.-, and PO.sub.2.sup.+ tetrahedral oxide units having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2 wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of zero to about 0.3 but is preferably not greater than about 0.15; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides. When "n" of CrO.sub.2.sup.n is equal to -1 or +1 the mole fractions "x", "y", and "z" are generally defined as being within the hexagonal compositional area defined by points A, B, C, D, E and F of the ternary diagram of FIG. 1. Points A, B, C, D, E and F of FIG. 1 have the following values for "x", "y", and "z": ______________________________________ Mole FractionPoint x y z______________________________________A 0.01 0.60 0.39B 0.01 0.39 0.60C 0.39 0.01 0.60D 0.60 0.01 0.39E 0.60 0.39 0.01F 0.39 0.60 0.01______________________________________ When "n" of CrO.sub.2.sup.n is zero (0) the mole fractions "x", "y", and "z" are generally defined as being within the pentagonal compositional area defined by points G, H, I, J and K of the ternary diagram of FIG. 2. Points G, H, I, J and K of FIG. 2 have the following values for "x", "y", and "z": ______________________________________ Mole FractionPoint x y z______________________________________G 0.01 0.60 0.39H 0.01 0.47 0.52I 0.94 0.01 0.05J 0.98 0.01 0.01K 0.39 0.60 0.01______________________________________

There are three preferred subclasses of the CAPO molecular sieves where the values of "x", "y" and "z" in the above formula depend on whether "n" of CrO.sub.2.sup.n is -1, 0 or +1. When "n" is -1, the preferred values of "x", "y" and "z" are within the tetragonal compositional area defined by the points, a, b, c and d of the ternary diagram which is FIG. 3 of the drawings, said points a, b, c and d representing the following values for "x", "y" and "z":

______________________________________ Mole FractionPoint x y z______________________________________a 0.01 0.59 0.40b 0.01 0.39 0.60c 0.39 0.01 0.60d 0.59 0.01 0.40______________________________________ Within this preferred subclass, an especially preferred subclass are those in which the values of "x", "y" and "z" in the formula are within the hexagonal compositional area defined by the points n, o, p, q, r, and s of the ternary diagram which is FIG. 3 of the drawings, said points n, o, p, q, r, and s representing the following values for "x", "y" and "z": ______________________________________ Mole FractionPoint x y z______________________________________n 0.01 0.52 0.47o 0.01 0.42 0.57p 0.03 0.40 0.57q 0.07 0.40 0.53r 0.07 0.47 0.46s 0.02 0.52 0.46______________________________________ When "n" of CrO.sub.2.sup.n is zero, the preferred values of "x", "y" and "z" are within the pentagonal compositional area defined by the points e, f, g and h of the ternary diagram which is FIG. 4 of the drawings, said points e, f, g and h representing the following values for "x", "y" and "z": ______________________________________Mole FractionPoint x y z______________________________________e 0.01 0.60 0.39f 0.01 0.47 0.52g 0.50 0.225 0.275h 0.50 0.40 0.10i 0.30 0.60 0.10______________________________________ When "n" of CrO.sub.2.sup.n is +1, the preferred values of "x", "y" and "z" are within the tetragonal compositional area defined by the points j, k, l and m of the ternary diagram which is FIG. 5 of the drawings, said points j, k, l and m representing the following values for "x", "y" and "z": ______________________________________ Mole FractionPoint x y z______________________________________j 0.01 0.60 0.39k 0.01 0.40 0.59l 0.59 0.40 0.01m 0.39 0.60 0.01______________________________________

The CAPO compositions preferably contain not more than about 0.5 moles of water per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2.

The CAPOs of this invention are useful as adsorbents, catalysts, ion-exchangers, and the like in much the same fashion as aluminosilicates have been employed heretofore, although their chemical and physical properties are not necessarily similar to those observed for aluminosilicates.

CAPO compositions are generally synthesized by hydrothermal crystallization from a reaction mixture containing reactive sources of chromium, aluminum and phosphorus, preferably an organic templating, i.e., structure-directing, agent, preferably a compound of an element of Group VA of the Periodic Table, and/or optionally an alkali or other metal. The reaction mixture is generally placed in a sealed pressure vessel, preferably lined with an inert plastic material such as polytetrafluoroethylene and heated, preferably under autogenous pressure, at a temperature between 50.degree. and 250.degree. C., and preferably between 100.degree. C. and 200.degree. C. until crystals of the CAPO product are obtained, usually a period of from several hours to several weeks. Typical crystallization times are from about 2 hours to about 30 days with from about 2 hours to about 20 days, and preferably about 1 to about 10 days, being generally employed to obtain crystals of the CAPO products. The product is recovered by any convenient method such as centrifugation or filtration.

In synthesizing the CAPO compositions of the instant invention, it is preferred to employ a reaction mixture composition expressed in terms of the molar ratios as follows:

aR:(Cr.sub.u Al.sub.v P.sub.w)O.sub.2 :bH.sub.2 O wherein "R" is an organic templating agent; "a" is the amount of organic templating agent "R" and has a value of from zero to about 6 and is preferably an effective amount within the range of greater than zero (0) to about 6 and most preferably not more than about 0.6; "b" has a value of from zero (0) to about 500, preferably between about 2 and about 300, most preferably not greater than about 20; and "u", "v" and "w" represent the mole fractions of chromium, aluminum and phosphorus, respectively, and each has a value of at least 0.01. The mole fractions "u", "v" and "w" in the reaction mixture are preferably within the pentagonal compositional area defined by points L, M, N, O and P which is shown in FIG. 6 of the drawings, where points L, M, N, O and P have the following values for "u", "v" and "w" : ______________________________________ Mole FractionPoint u v w______________________________________L 0.01 0.60 0.39M 0.01 0.39 0.60N 0.39 0.01 0.60O 0.98 0.01 0.01P 0.39 0.60 0.01______________________________________

Especially preferred reaction mixture compositions are those containing from about 0.1 to about 0.4 moles of chromium, and from about 0.75 to about 1.25 moles of aluminum, per mole of phosphorus.

In the foregoing expression of the reaction composition, the reactants are normalized with respect to the total of x+y+z=1.00 mole, whereas in the examples the reaction mixtures are expressed in terms of the molar oxide ratios and may be normalized to 1.00 mole of Al.sub.2 O.sub.3 or P.sub.2 O.sub.5. This latter form is readily converted to the former form by routine calculation by dividing the total number of moles of chromium, aluminum and phosphorus into the moles of each of the aforementioned elements chromium, aluminum and phosphorus. The moles of template and water are similarly normalized by dividing by the total moles of chromium, phosphorus and aluminum.

In forming the reaction mixture from which the instant molecular sieves are formed the organic templating agent can be any of those heretofore proposed for use in the synthesis of conventional zeolite aluminosilicates. In general these compounds contain elements of Group VA of the Periodic Table of Elements, particularly nitrogen, phosphorus, arsenic and antimony, preferably nitrogen or phosphorus and most preferably nitrogen, which compounds also contain at least one alkyl or aryl group having from 1 to 8 carbon atoms. Particularly preferred compounds for use as templating agents are the amines, quaternary phosphonium and quaternary ammonium compounds, the latter being represented generally by the formula R.sub.4 X.sup.+ wherein "X" is nitrogen or phosphorus and each R is an alkyl or aryl group containing from 1 to 8 carbon atoms. Polymeric quaternary ammonium salts such as [(C.sub.14 H.sub.32 N.sub.2)(OH).sub.2 ].sub.x wherein "x" has a value of at least 2 are also suitably employed. The mono-, di- and tri-amines are advantageously utilized, either alone or in combination with a quarternary ammonium compound or other templating compound. Mixtures of two or more templating agents can either produce mixtures of the desired CAPOs or the more strongly directing templating species may control the course of the reaction with the other templating species serving primarily to establish the pH conditions of the reaction gel. Representative templating agents include tetramethylammonium, tetraethylammonium, tetrapropylammonium or tetrabutylammonium ions; tetrapentylammonium ion; di-n-propylamine; tripropylamine; triethylamine; triethanolamine; piperidine; cyclohexylamine; 2-methylpyridine; N,N-dimethylbenzylamine; N,N-dimethylethanolamine; choline; N,N'-dimethylpiperazine; 1,4-diazabicyclo(2,2,2,)octane; N-methyldiethanolamine, N-methylethanolamine; N-methylpiperidine; 3-methylpiperidine; N-methylcyclohexylamine; 3-methylpyridine; 4-methylpyridine; quinuclidine; N,N'-dimethyl-1,4-diazabicyclo(2,2,2)octane ion; di-n-butylamine, neopentylamine; di-n-pentylamine; isopropylamine; t-butylamine; ethylenediamine; pyrrolidine; and 2-imidazolidone. Not every templating agent will direct the formation of every species of CAPO, i.e., a single templating agent can, with proper manipulation of the reaction condition, direct the formation of several CAPO compositions, and a given CAPO composition can be produced using several different templating agents.

The reactive phosphorus source is preferably phosphoric acid, but organic phosphates such as triethyl phosphate may be satisfactory, and so also may crystalline or amorphous aluminophosphates such as the AlPO.sub.4 composition of U.S. Pat. No. 4,310,440. Organo-phosphorus compounds, such as tetrabutylphosphonium bromide, do not apparently serve as reactive sources of phosphorus, but these compounds may function as templating agents. Conventional phosphorus salts such as sodium metaphosphate, may be used, at least in part, as the phosphorus source, but are not preferred.

The preferred aluminum source is either an aluminum alkoxide, such as aluminum isoproproxide, aluminum chlorhydrol (Al.sub.2 (OH).sub.5 Cl.2.5H.sub.2 O) or pseudoboehmite. The crystalline or amorphous aluminophosphates which are a suitable source of phosphorus are, of course, also suitable sources of aluminum. Other sources of aluminum used in zeolite synthesis, such as gibbsite, sodium aluminate and aluminum trichloride, can be employed but are not preferred.

The reactive source of chromium can be introduced into the reaction system in any form which permits the formation in situ of a reactive form of chromium, i.e., reactive to form the framework tetrahedral oxide unit of chromium. Compounds of chromium which may be employed include oxides, alkoxides, hydroxides, chlorides, bromides, iodides, nitrates, sulfates, carboxylates (e.g., acetates) and the like. Especially preferred sources of chromium are chromium(III) orthophosphate, chromium(III) acetate and chromium acetate hydroxide (Cr.sub.3 (OH).sub.2 (CH.sub.3 COO).sub.7).

While not essential to the synthesis of CAPO compositions, stirring or other moderate agitation of the reaction mixture and/or seeding the reaction mixture with seed crystals of either the CAPO species to be produced or a topologically similar aluminophosphate, aluminosilicate or molecular sieve composition, facilitates the crystallization procedure.

After crystallization the CAPO product may be isolated and advantageously washed with water and dried in air. The as-synthesized CAPO generally contains within its internal pore system at least one form of the templating agent employed in its formation. Most commonly the organic moiety is present, at least in part, as a charge-balancing cation as is generally the case with as-synthesized aluminosilicate zeolites prepared from organic-containing reaction systems. It is possible, however, that some or all of the organic moiety is an occluded molecular species in a particular CAPO species. As a general rule the templating agent, and hence the occluded organic species, is too large to move freely through the pore system of the CAPO product and must be removed by calcining the CAPO at temperatures of 200.degree. C. to 700.degree. C., preferably about 350.degree. C. to about 600.degree. C., to thermally degrade the organic species. In a few instances the pores of the CAPO product are sufficiently large to permit transport of the templating agent, particularly if the latter is a small molecule, and accordingly complete or partial removal thereof can be accomplished by conventional desorption procedures such as carried out in the case of zeolites. It will be understood that the term "as-synthesized" as used herein does not include the condition of the CAPO phase wherein the organic moiety occupying the intracrystalline pore system as a result of the hydrothermal crystalline process has been reduced by post-synthesis treatment such that the value of "m" in the composition formula

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2 has a value of less than 0.02. The other symbols of the formula are as defined hereinabove. In those preparations in which an alkoxide is employed as the source of chromium, aluminum or phosphorus, the corresponding alcohol is necessarily present in the reaction mixture since it is a hydrolysis product of the alkoxide. It has not been determined whether this alcohol participates in the synthesis process as a templating agent. For the purposes of this application, however, this alcohol is arbitarily omitted from the class of templating agents, even if it is present in the as-synthesized CAPO material.

Since the present CAPO compositions are formed from CrO.sub.2, AlO.sub.2 and PO.sub.2, tetrahedral units which, respectively, have a net charge of "n" (-1, 0 or +1), -1 and +1, the matter of cation exchangeability is considerably more complicated than in the case of zeolitic molecular sieves in which, ideally, there is a stoichiometric relationship between AlO.sub.2.sup.- tetrahedra and charge-balancing cations. In the instant compositions, an AlO.sub.2.sup.- tetrahedron can be balanced electrically either by association with a PO.sub.2.sup.+ tetrahedron or a simple cation such as an alkali metal cation, a proton (H.sup.+), a cation of chromium present in the reaction mixture, or an organic cation derived from the templating agent. Similarly, an CrO.sub.2.sup.- tetrahedron can be balanced electrically by association with PO.sub.2.sup.+ tetrahedra, a cation of chromium present in the reaction mixture, organic cations derived from the templating agent, a simple cation such as an alkali metal cation, a proton (H.sup.+), or other divalent or polyvalent metal cations introduced from an extraneous source. It has also been postulated that non-adjacent AlO.sub.2.sup.- and PO.sub.2.sup.+ tetrahedral pairs can be balanced by Na.sup.+ and OH.sup.- respectively [Flanigen and Grose, Molecular Sieve Zeolites-I, ACS, Washington, DC (1971)].

The CAPO compositions of the present invention may exhibit cation-exchange capacity when analyzed using ion-exchange techniques heretofore employed with zeolitic aluminosilcates and have pore diameters which are inherent in the lattice structure of each species and which are at least about 3 .ANG. in diameter. Ion exhange of CAPO compositions is ordinarily possible only after any organic moiety derived from the template, present as a result of synthesis, has been removed from the pore system. Dehydration to remove water present in the as-synthesized CAPO compositions can usually be accomplished, to some degree at least, in the usual manner without removal of the organic moiety, but the absence of the organic species greatly facilitates adsorption and desorption procedures. The CAPO materials have various degrees of hydrothermal and thermal stability, some being quite remarkable in this regard, and function well as molecular sieve adsorbents and hydrocarbon conversion catalysts or catalyst bases.

In preparing the CAPO composition it is preferred to use a stainless steel reaction vessel lined with an inert plastic material, e.g., polytetrafluoroethylene, to avoid contamination of the reaction mixture. In general, the final reaction mixture from which each CAPO composition is crystallized is prepared by forming mixtures of less than all of the reagents and thereafter incorporating into these mixtures additional reagents either singly or in the form of other intermediate mixtures of two or more reagents. In some instances the reagents admixed retain their identity in the intermediate mixture and in other cases some or all of the reagents are involved in chemical reactions to produce new reagents. The term "mixture" is applied in both cases. Further, it is preferred that the intermediate mixtures as well as the final reaction mixtures be stirred until substantially homogeneous.

X-ray patterns of reaction products are obtained by X-ray analysis using either: (1) copper K-alpha radiation, Siemens Type K-805 X-ray sources and computer interfaced Seimen's D-500 X-ray powder diffractometers, available from Seimens Corporation, Cherry Hill, N.J.; or (2) standard X-ray powder diffraction techniques. When the standard technique is employed the radiation source is a high-intensity, copper target, X-ray tube operated at 50 Kv and 40 ma. The diffraction pattern from the copper K-alpha radiation and graphite monochromator is suitably recorded by an X-ray spectrometer scintillation counter, pulse height analyzer and strip chart recorder. X-ray patterns are obtained using flat compressed powder samples which are scanned at 2.degree. (2 theta) per minute, using a two second time constant.

All interplanar spacings (d) in Angstrom units are obtained from the position of the diffraction peaks expressed as 2.theta. where .theta. is the Bragg angle as observed on the strip chart. Intensities are determined from the heights of diffraction peaks after subtracting background, "I.sub.o " being the intensity of the strongest line or peak, and "I" being the intensity of each of the other peaks.

As will be understood by those skilled in the art the determination of the parameter 2 theta is subject to both human and mechanical error, which in combination, can impose an uncertainty of about .+-.0.4.degree. on each reported value of 2 theta. This uncertainty is, of course, also manifested in the reported values of the d-spacings, which are calculated from the 2 theta values. This imprecision is general throughout the art and is not sufficient to preclude the differentiation of the present crystalline materials from each other and from the compositions of the prior art. In some of the X-ray patterns reported, the relative intensities of the d-spacings are indicated by the notations vs, s, m, w and vw which represent very strong, strong, medium, weak and very weak, respectively.

In certain instances the purity of a synthesized product may be assessed with reference to its X-ray powder diffraction pattern. Thus, for example, if a sample is stated to be pure, it is intended only that the X-ray pattern of the sample is free of lines attributable to crystalline impurities, not that there are no amorphous materials present.

The molecular sieves of the instant invention may be characterized by their X-ray powder diffraction patterns and as such may have one of the X-ray patterns set forth in the following Tables A through V, wherein said X-ray patterns are for the as-synthesized form unless otherwise noted. In most cases, the pattern of the corresponding calcined form will also fall within the relevant Table. However, in some cases the removal of the occluded templating agent which occurs during calcination will be accompanied by sufficient relaxation of the lattice to shift some of the lines slightly outside the ranges specified in the relevant Table. In a small number of cases, calcination appears to cause more substantial distortions in the crystal lattice, and hence more significant changes in the X-ray powder diffraction pattern.

TABLE A______________________________________(CAPO-5)2.theta. d(.ANG.) Relative Intensity______________________________________ 7.3-7.65 12.1-11.56 m-vs19.5-20.0 4.55-4.44 m-s20.9-21.3 4.25-4.17 m-vs22.2-22.6 4.00-3.93 w-vs25.7-26.2 3.47-3.39 w-m______________________________________ TABLE B______________________________________(CAPO-11)2.theta. d(.ANG.) Relative Intensity______________________________________ 9.3-9.65 9.51-9.17 m-s20.2-20.6 4.40-4.31 m-s20.9-21.3 4.25-4.17 s-vs22.0-22.5 4.04-3.95 m-s22.5-22.9 3.95-3.92 m-s23.0-23.4 3.87-3.80 m-vs______________________________________ TABLE C______________________________________(CAPO-14)2.theta. d(.ANG.) Relative Intensity______________________________________8.6-8.9 10.3-9.93 vs13.0 6.81 w21.9-22.2 4.06-4.00 w25.4 3.51 w27.5 3.24 w29.7 3.01 w______________________________________ TABLE D______________________________________(CAPO-16)2.theta. d(.ANG.) Relative Intensity______________________________________11.3-11.6 7.83-7.63 m-vs18.7-18.9 4.75-4.70 w-s21.9-22.3 4.06-3.99 m-vs26.5-27.0 3.363-3.302 w-m 29.7-30.05 3.008-2.974 w-m______________________________________ TABLE E______________________________________(CAPO-17)2.theta. d(.ANG.) Relative Intensity______________________________________ 7.7-7.75 11.5-11.4 vs13.4 6.61 s-vs 15.5-15.55 5.72-5.70 s19.65-19.7 4.52-4.51 w-s20.5-20.6 4.33-4.31 vs 31.8-32.00 2.812-2.797 w-s______________________________________ TABLE F______________________________________(CAPO-18)2.theta. d(.ANG.) Relative Intensity______________________________________9.5-9.7 9.23-9.16 vs15.4-15.6 5.76-5.66 m16.9-17.1 5.25-5.19 m20.15-20.3 4.41-4.38 m20.95-21.1 4.24-4.20 m31.8-32.6 2.814-2.749 m______________________________________ TABLE G______________________________________(CAPO-20)2.theta. d(.ANG.) Relative Intensity______________________________________ 13.7-14.25 6.46-6.22 m-vs19.55-20.0 4.54-4.44 w-s24.05-24.5 3.70-3.63 m-vs34.3-35.0 2.614-2.564 vw-w42.5-43.0 2.127-2.103 vw-w______________________________________ TABLE H______________________________________(CAPO-31)2.theta. d(.ANG.) Relative Intensity______________________________________8.5-8.6 10.40-10.28 m-s20.2-20.3 4.40-4.37 m21.9-22.1 4.06-4.02 w-m22.6-22.7 3.93-3.92 vs31.7-31.8 2.823-2.814 w-m______________________________________ TABLE J*______________________________________(CAPO-33)2.theta. d(.ANG.) Relative Intensity______________________________________9.25-9.55 9.56-9.26 w-m12.5-12.9 7.08-6.86 vs16.9-17.3 5.25-5.13 w-m20.45-20.9 4.34-4.25 w-m23.85-24.25 3.73-3.67 w-m26.05-26.35 3.42-3.38 w-m27.3-27.6 3.27-3.23 vs______________________________________ *as-synthesized form TABLE K*______________________________________(CAPO-33)2.theta. d(.ANG.) Relative Intensity______________________________________13.15-13.4 6.73-6.61 vs18.05-18.35 4.91-4.83 m18.4-18.6 4.82-4.77 m26.55-26.7 3.36-3.34 m32.0-32.1 2.80-2.79 m______________________________________ *calcined form TABLE L______________________________________(CAPO-34)2.theta. d(.ANG.) Relative Intensity______________________________________ 9.4-9.65 9.41-9.17 s-vs15.9-16.2 5.57-5.47 vw-m17.85-18.4 4.97-4.82 w-s20.3-20.9 4.37-4.25 m-vs24.95-25.4 3.57-3.51 vw-s30.3-30.8 2.95-2.90 w-s______________________________________ TABLE M______________________________________(CAPO-35)2.theta. d(.ANG.) Relative Intensity______________________________________10.8-11.1 8.19-7.97 m17.2-17.4 5.16-5.10 s-vs 21.0-21.25 4.23-4.18 m-s21.8-22.0 4.08-4.04 vs31.8-32.2 2.814-2.788 m______________________________________ TABLE N______________________________________(CAPO-36)2.theta. d(.ANG.) Relative Intensity______________________________________7.7-7.9 11.5-11.2 vs16.2-16.6 5.47-5.34 w-m18.9-19.3 4.70-4.60 m-s20.6-20.8 4.31-4.27 w-s21.8-22.0 4.08-4.04 m22.2-22.5 4.00-3.95 w-m______________________________________ TABLE O______________________________________(CAPO-37)2.theta. d(.ANG.) Relative Intensity______________________________________6.1-6.3 14.49-14.03 vs15.5-15.7 5.72-5.64 w-m18.5-18.8 4.80-4.72 w-m23.5-23.7 3.79-3.75 w-m26.9-27.1 3.31-3.29 w-m______________________________________ TABLE P______________________________________(CAPO-39)2.theta. d(.ANG.) Relative Intensity______________________________________9.4-9.6 9.41-9.21 w-m13.3-13.6 6.66-6.51 m-vs18.0-18.4 4.93-4.82 m21.2-21.5 4.19-4.13 m-s22.5-23.0 3.95-3.87 s-vs30.2-30.5 2.96-2.93 w-m______________________________________ TABLE Q______________________________________(CAPO-40)2.theta. d(.ANG.) Relative Intensity______________________________________7.5-7.7 11.79-11.48 vw-m8.0-8.1 11.05-10.94 s-vs12.4-12.5 7.14-7.08 w-vs13.6-13.8 6.51-6.42 m-s14.0-14.1 6.33-6.28 w-m27.8-28.0 3.209-3.187 w-m______________________________________ TABLE R______________________________________(CAPO-41)2.theta. d(.ANG.) Relative Intensity______________________________________13.6-13.9 6.51-6.38 w-m21.1-21.3 4.21-4.17 vs22.1-22.4 4.02-3.97 m-s23.0-23.4 3.87-3.80 w-m25.5-26.0 3.493-3.440 w-m______________________________________ TABLE S______________________________________(CAPO-42)2.theta. d(.ANG.) Relative Intensity______________________________________7.15-7.4 12.36-11.95 m-vs12.5-12.7 7.08-6.97 m-s21.75-21.9 4.09-4.06 m-s 24.1-24.25 3.69-3.67 vs27.25-27.4 3.273-3.255 s30.05-30.25 2.974-2.955 m-s______________________________________ TABLE T______________________________________(CAPO-44)2.theta. d(.ANG.) Relative Intensity______________________________________ 9.4-9.55 9.41-9.26 vs13.0-13.1 6.81-6.76 w-m16.0-16.2 5.54-5.47 w-m 20.6-20.85 4.31-4.26 s-vs24.3-24.4 3.66-3.65 w-vs 30.7-30.95 2.912-2.889 w-s______________________________________ TABLE U______________________________________(CAPO-46)2.theta. d(.ANG.) Relative Intensity______________________________________7.2-8.1 12.3-10.9 vs21.2-21.8 4.19-4.08 w-m22.5-23.0 3.95-3.87 vw-m26.6-27.2 3.351-3.278 vw-w28.5-29.0 3.132-3.079 vw-w______________________________________ TABLE V______________________________________(CAPO-47)2.theta. d(.ANG.) Relative Intensity______________________________________9.4 9.41 vs15.9-16.0 5.57-5.54 w-m20.5-20.6 4.33-4.31 s24.5-24.7 3.63-3.60 w25.8-25.9 3.45-3.44 w30.4-30.5 2.940-2.931 w.______________________________________

The exact nature of the CAPO molecular sieves is not entirely understood at present, although all are believed to contain CrO.sub.2 tetrahedra in the three-dimensional microporous crystal framework structure. The low level of chromium present in some of the instant molecular sieves prepared to date makes it difficult to ascertain the exact nature of the interaction among chromium, aluminum and phosphorus. As a result, although it is believed that CrO.sub.2 tetrahedra are substituted isomorphously for AlO.sub.2 or PO.sub.2 tetrahedra, it is appropriate to characterize certain CAPO compositions by reference to their chemical compositions in terms of the molar ratios of oxides, as has been done in some of the examples below.

The following examples are provided to further illustrate the invention and are not intended to be limiting thereof:

EXAMPLE 1

(Preparation of CAPO-5)

An initial mixture was prepared by adding 29.3 grams of aluminum chlorhydrol (Al.sub.2 (OH).sub.5 Cl.2H.sub.2 O) to a solution prepared by dissolving 1.4 grams of chromium acetate hydroxide (Cr.sub.3 (OH).sub.2 (CH.sub.3 COO).sub.7) in 29.0 grams of water. To this initial mixture were added 15.4 grams of 85% orthophosphoric acid, and to the resultant mixture were added 12.3 grams of a 40 wt. percent aqueous solution of tetraethylammonium hydroxide (TEAOH), followed by 13.5 grams of n-dipropylamine (n-Pr.sub.2 NH). The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

0.5TEAOH:2.0n-Pr.sub.2 NH:0.1Cr.sub.2 O.sub.3 :1.0Al.sub.2 O.sub.3 :1.0P.sub.2 O.sub.5 :50H.sub.2 O.

This final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 68 hours. The solid reaction product (which was determined by the analyses described below to be mainly CAPO-5) was recovered by centrifugation, washed with water and dried in air at ambient temperature.

A sample of this solid reaction product was analyzed and the following chemical analysis obtained:

______________________________________Component Weight percent______________________________________Carbon 6.4Nitrogen 1.0Cr.sub.2 O.sub.3 1.3Al.sub.2 O.sub.3 33.6P.sub.2 O.sub.5 53.0LOI* 12.9______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.22(TEAOH+n-Pr.sub.2 NH):0.03Cr.sub.2 O.sub.3 :1.00Al.sub.2 O.sub.3 :1.13P.sub.2 O.sub.5 :0.52H.sub.2 O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.07(TEAOH+n-Pr.sub.2 NH):(Cr.sub.0.01 Al.sub.0.46 P.sub.0.53)O.sub.2

Microprobe analysis of crystals having the morphology expected for CAPO-5 indicated the following relative proportions of chromium, aluminum and phosphorus:

Cr.sub.0.02 Al.sub.0.48 P.sub.0.51 so that the product contained chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1.

The product was not pure, but the X-ray powder diffraction pattern of the major phase, as synthesized, was characterized by the data in the following Table AA (Hereinafter, Tables designated AA, AB etc. represent Tables containing all the peaks set forth in Table A above, and similarly for Tables BA, BB etc.):

TABLE AA______________________________________(CAPO-5) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________7.4 11.89 10012.9 6.84 815.0 5.92 2019.8 4.47 4421.0 4.23 4722.5 3.95 6424.8 3.59 326.1 3.41 2129.1 3.07 930.2 2.956 1233.8 2.656 434.8 2.580 1037.1 2.421 337.8 2.382 941.8 2.159 248.0 1.893 3______________________________________

EXAMPLE 2

(Preparation of CAPO-5)

(a) A solution was formed by dissolving 23.2 grams of 85 wt. percent orthophosphoric acid (H.sub.3 PO.sub.4) in 41.1 grams of water. The resultant solution was combined with 13.6 grams of hydrated aluminum oxide in the form of a pseudo-boehmite phase comprising 75.1 wt. percent of Al.sub.2 O.sub.3 and 24.9 wt. percent of H.sub.2 O. Separately, 2.1 grams of chromium acetate hydroxide (Cr.sub.3 (OH).sub.2 (CH.sub.3 COO).sub.7) were dissolved in 20.1 grams of water, and then the resultant solution was added to the previously-prepared mixture. To the resultant mixture were added 37.0 grams of a 40 wt. percent aqueous solution of tetraethylammonium hydroxide (TEAOH), and the resultant mixture was mixed until homogeneous. The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

1.0TEAOH:0.1Cr.sub.2 O.sub.3 :0.9Al.sub.2 O.sub.3 :1.0P.sub.2 O.sub.5 :50H.sub.2 o.

This final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 150.degree. C. under autogeneous pressure for 48 hours. The solid reaction product (which was determined by the analyses described below to be mainly CAPO-5) was recovered by filtration, washed with water and dried in air at ambient temperature.

A sample of this solid reaction product was analyzed and the following chemical analysis obtained:

______________________________________Component Weight percent______________________________________Carbon 5.8Nitrogen 0.7Cr.sub.2 O.sub.3 2.1Al.sub.2 O.sub.3 33.7P.sub.2 O.sub.5 47.5LOI* 15.4______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.15TEAOH:0.04Cr.sub.2 O.sub.3 :1.00Al.sub.2 O.sub.3 :1.02P.sub.2 O.sub.5 :1.09H.sub.2 O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.06TEAOH:(Cr.sub.0.02 Al.sub.0.49 P.sub.0.49)O.sub.2

Microprobe analysis of crystals having the morphology expected for CAPO-5 indicated the following relative proportions of chromium, aluminum and phosphorus:

Cr.sub.0.03 Al.sub.0.43 P.sub.0.54 so that the product contained chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1.

The product was not pure, but the X-ray powder diffraction pattern of the major phase was substantially the same as that given in Table AA above.

The X-ray powder diffraction pattern of the major phase, after calcination by heating to 600.degree. C. in air for 3.5 hours, was characterized by the data in the following Table AB:

TABLE AB______________________________________(CAPO-5) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________7.5 11.83 10013.0 6.83 2119.9 4.47 2221.2 4.19 4522.5 3.94 6324.9 3.57 326.1 3.42 2029.2 3.06 1630.2 2.963 1233.9 2.645 434.7 2.587 1038.0 2.368 6______________________________________

(b) A sample of the calcined product produced in part (a) was utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus. Before being used in the adsorption tests, the sample was activated by heating to 350.degree. C. overnight in vacuum. The following data were generated in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed______________________________________O2 3.46 103.0 -183 15.8O2 3.46 730.0 -183 23.3Neopentane 6.2 100.0 23.8 6.4Neopentane 6.2 746.0 29.3 8.9H2O 2.65 4.6 23.4 14.3H2O 2.65 20 23.5 28.9______________________________________

From the above data, the pore size of the calcined product was determined to be greater than or equal to 6.2 .ANG., as shown by the adsorption of neopentane (kinetic diameter of 6.2 .ANG.).

X-ray analysis of the sample used in the adsorption studies showed that the powder X-ray diffraction pattern of the sample was essentially unchanged as a result of contact with the adsorbates.

EXAMPLE 3

(Preparation of CAPO-5)

A solution was formed by dissolving 24.1 grams of 85 wt. percent orthophosphoric acid (H.sub.3 PO.sub.4) in 46.2 grams of water. The solution was then mixed with 35.6 grams of aluminum isopropoxide (Al(OC.sub.3 H.sub.7).sub.3). The resultant solution was combined with a solution prepared by dissolving 4.9 grams of chromium(III) acetate (Cr(CH.sub.3 COO).sub.3) in 20.6 grams of water. To the resultant mixture was added a solution of 11.1 grams of quinuclidine (QN) in 20.7 grams of water, and the resultant mixture was stirred until homogeneous. The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

1.0QN:0.1Cr.sub.2 O.sub.3 :0.9Al.sub.2 O.sub.3 :1.0P.sub.2 O.sub.5 :50H.sub.2 O.

This final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 168 hours. The solid reaction product (which was determined by the analyses described below to be mainly CAPO-5) was recovered by centrifugation, washed with water and dried in air at ambient temperature.

A sample of this solid reaction product was analyzed and the following chemical analysis obtained:

______________________________________Component Weight percent______________________________________Carbon 10.6Nitrogen 1.6Cr.sub.2 O.sub.3 3.0Al.sub.2 O.sub.3 29.2P.sub.2 O.sub.5 45.9LOI* 23.1______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.40QN:0.07Cr.sub.2 O.sub.3 :1.00Al.sub.2 O.sub.3 :1.13P.sub.2 O.sub.5 :1.77H.sub.2 O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.10QN:(Cr.sub.0.03 Al.sub.0.46 P.sub.0.51)O.sub.2

Microprobe analysis of crystals having the morphology expected for CAPO-5 indicated the following relative proportions of chromium, aluminum and phosphorus:

Cr.sub.0.02 Al.sub.0.44 P.sub.0.54 so that the product contained chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1.

The X-ray powder diffraction pattern of the composition was substantially the same as that given in Table AA above.

EXAMPLE 4

(Preparation of CAPO-5)

A solution was formed by dissolving 23.3 grams of 85 wt. percent orthophosphoric acid (H.sub.3 PO.sub.4) in 53.6 grams of water. The resultant solution was combined with 13.6 grams of hydrated aluminum oxide in the form of a pseudo-boehmite phase comprising 75.1 wt. percent of Al.sub.2 O.sub.3 and 24.9 wt. percent of H.sub.2 O. Separately, 2.1 grams of chromium acetate hydroxide (Cr.sub.3 (OH).sub.2 (CH.sub.3 COO).sub.7) were dissolved in 31.1 grams of water, and then the resultant solution was added to the previously-prepared mixture. To the resultant mixture was added 14.3 grams of tripropylamine (Pr.sub.3 N), and the resultant mixture was mixed until homogeneous. The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

1.0Pr.sub.3 N:0.1Cr.sub.2 O.sub.3 :0.9Al.sub.2 O.sub.3 :1.0P.sub.2 O.sub.5 :50H.sub.2 O.

An aliquot of this final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 72 hours. The solid reaction product (which was determined by X-ray analysis to be mainly CAPO-5) was recovered by filtration, washed with water and dried in air at ambient temperature.

The X-ray powder diffraction pattern of the composition thus produced was substantially the same as that given in Table AA above.

A further aliquot of the final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 168 hours. The solid reaction product (which was determined by X-ray analysis to be mainly CAPO-5) was recovered by filtration, washed with water and dried in air at ambient temperature.

______________________________________Component Weight percent______________________________________Carbon 6.0Nitrogen 0.9Cr.sub.2 O.sub.3 2.0Al.sub.2 O.sub.3 35.1P.sub.2 O.sub.5 51.5LOI* 10.1______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.19Pr.sub.3 N:0.04Cr.sub.2 O.sub.3 :1.00Al.sub.2 O.sub.3 :1.06P.sub.2 O.sub.5 :0.34H.sub.2 O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.04P.sub.13 N:(Cr.sub.0.02 Al.sub.0.48 P.sub.0.50)O.sub.2

The X-ray powder diffraction pattern of the composition thus produced was substantially the same as given in Table AA above.

The following general Table AC summarizes the X-ray powder diffraction lines which were obtained from the specimens of CAPO-5 prepared in Examples 1-4 above. The least intense lines were not obtained from every specimen.

TABLE AC______________________________________(CAPO-5) Relative Intensity2.theta. D(.ANG.) 100 .times. I/I.sub.o______________________________________7.4-7.6 11.63-11.95 10012.9-13.1 6.75-6.88 6-2114.9-15.1 5.86-5.95 14-2419.7-20.0 4.44-4.50 21-5120.9-21.2 4.19-4.25 3-7722.4-22.6 3.93-3.97 14-6824.6-25.0 3.56-3.62 1-626.0-26.2 3.39-3.43 12-2629.0-29.2 3.05-3.08 2-1630.1-30.4 2.944-2.970 12-1933.7-33.9 2.645-2.661 1-434.6-34.9 2.570-2.593 1-1236.9-37.2 2.415-2.434 1-337.6-38.0 2.368-2.395 1-1041.7-41.9 2.154-2.168 1-347.8-48.2 1.890-1.902 1-5______________________________________

EXAMPLE 5

(Preparation of CAPO-11)

An initial mixture was formed by mixing 4.2 grams of chromium acetate hydroxide (Cr.sub.3 (OH).sub.2 (CH.sub.3 COO).sub.7 with 27.2 grams of hydrated aluminum oxide in the form of a pseudo-boehmite phase comprising 75.1 wt. percent of Al.sub.2 O.sub.3 and 24.9 wt. percent of H.sub.2 O. This dry mixture was added very slowly to 46.3 grams of 85 wt. percent orthophosphoric acid (H.sub.3 PO.sub.4) in an ice bath. To the resultant mixture was added 40.4 grams of di-n-propylamine (n-Pr.sub.2 NH), and the mixture was mixed until homogeneous. The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

2.0n-Pr.sub.2 NH:0.1Cr.sub.2 O.sub.3 :1.00Al.sub.2 O.sub.3 :1.0P.sub.2 O.sub.5 :6.8H.sub.2 O.

This final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 96 hours. The solid reaction product (which was determined by the analyses described below to be mainly CAPO-11) was recovered by centrifugation, washed with water and dried in air at ambient temperature.

A sample of this solid reaction product was analyzed and the following chemical analysis obtained:

______________________________________Component Weight percent______________________________________Carbon 4.8Nitrogen 1.0Cr.sub.2 O.sub.3 1.9Al.sub.2 O.sub.3 35.6P.sub.2 O.sub.5 50.7LOI* 12.5______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.20n-Pr.sub.2 NH:0.04Cr.sub.2 O.sub.3 :1.00Al.sub.2 O.sub.3 :1.02P.sub.2 O.sub.5 :0.88H.sub.2 O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.05n-Pr.sub.2 NH:(Cr.sub.0.02 Al.sub.0.49 P.sub.0.50)O.sub.2

Microprobe analysis of crystals having the morphology expected for CAPO-11 indicated the following relative proportions of chromium, aluminum and phosphorus:

Cr.sub.0.01 Al.sub.0.48 P.sub.0.51 so that the product contained chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1.

The product was not pure, but the X-ray powder diffraction pattern of the major phase, as synthesized, was characterized by the data in the following Table BA:

TABLE BA______________________________________(CAPO-11) Relative Intensity2.theta. d(.ANG.) 100 .times. I/I.sub.o______________________________________8.1 10.91 239.4 9.36 6613.2 6.70 1115.7 5.65 2716.3 5.43 419.0 4.66 620.5 4.34 3021.0 4.22 10022.2 4.01 4722.6 3.94 4422.7 3.91 4723.2 3.83 5524.7 3.60 726.4 3.38 1126.6 3.34 1128.7 3.11 1429.6 3.02 631.5 2.837 733.0 2.718 1034.3 2.616 736.6 2.456 337.6 2.389 837.9 2.376 1242.8 2.111 445.1 2.010 349.0 1.860 350.8 1.798 3______________________________________

Other specimens of CAPO-11 prepared in a similar manner had similar X-ray powder diffraction patterns. The following general Table BB summarizes the X-ray powder diffraction lines which were obtained from the various specimens of CAPO-11; the least intense lines were not obtained from every specimen.

TABLE BB______________________________________(CAPO-11) Relative Intensity2.theta. d(.ANG.) 100 .times. I/I.sub.o______________________________________8.1-8.2 10.76-10.94 19-399.4-9.6 9.23-9.38 53-6613.2-13.3 6.64-6.70 9-1715.7-15.8 5.60-5.65 21-3516.3-16.4 5.41-5.44 2-519.0-19.2 4.63-4.67 620.5-20.6 4.32-4.34 23-4621.0-21.2 4.19-4.22 10022.2-22.3 3.98-4.01 43-5122.6-22.7 3.92-3.94 33-6522.7-22.9 3.88-3.92 37-5623.2-23.4 3.81-3.83 47-6724.7-24.9 3.58-3.60 5-826.4-26.5 3.36-3.38 9-1226.6-26.7 3.33-3.34 9-1528.7-28.8 3.10-3.11 12-1429.6-29.7 3.01-3.02 6-931.5-31.7 2.825-2.837 7-1033.0-33.1 2.708-2.718 9-1334.3-34.4 2.605-2.616 5-1036.6-36.7 2.449-2.456 3-437.6 2.389-2.391 7-837.9-38.0 2.371-2.376 9-1242.8-43.0 2.102-2.111 3-445.1-45.2 2.004-2.011 2-448.9-49.0 1.860-1.861 2-350.8-51.0 1.792-1.798 3______________________________________

EXAMPLE 6

(Preparation of CAPO-17)

(a) CAPO-17 is prepared from a reaction mixture having a composition, expressed in terms of the molar oxide ratios of the components of the reaction mixture, of:

1.0-2.0QN:0.05-0.2Cr.sub.2 O.sub.q :0.5-1.0Al.sub.2 O.sub.3 :0.5-1.0P.sub.2 O.sub.5 :40-100H.sub.2 O where "QN" denotes quinuclidine and "q" denotes the oxidation state of chromium.

The reaction mixture is digested by placing the reaction mixture in a sealed stainless steel pressure vessel and heating it at an effective temperature and for an effective time until crystals of the CAPO-17 product are obtained. Solids are then recovered by filtration, washed with water and dried in air at room temperature.

The CAPO-17 product's chemical analysis shows the CAPO-17 product contains chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C., E and F of FIG. 1.

The X-ray powder diffraction pattern of a CAPO-17 product is characterized by the following data:

______________________________________2.theta. d(.ANG.) Relative Intensity______________________________________7.7-7.75 11.5-11.4 vs13.4 6.61 s-vs15.5-15.55 5.72-5.70 s19.65-19.7 4.52-4.51 w-s20.5-20.6 4.33-4.31 vs31.8-32.00 2.812-2.797 w-s______________________________________

(b) The X-ray powder diffraction pattern for a calcined CAPO-17 is also characterized by the X-ray pattern of part (a).

(c) When the calcined CAPO-17 of part (b) is utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus the measurements are made on a sample after activation at 350.degree. C. in a vacuum. The following data are used in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed*______________________________________O.sub.2 3.46 100 -183 10O.sub.2 3.46 750 -183 12n-Butane 4.3 100 24 4H.sub.2 O 2.65 4.3 24 13H.sub.2 O 2.65 20 24 14______________________________________ *typical amount adsorbed The pore diameter of CAPO-17 is about 4.3 .ANG..

EXAMPLE 7

(Preparation of CAPO-31)

(a) CAPO-31 is prepared from a reaction mixture having a composition, expressed in terms of the molar oxide ratios of the components of the reaction mixture, of:

1.0-2.0 DPA:0.05-0.2 Cr.sub.2 O.sub.q :0.5-1.0 Al.sub.2 O.sub.3 :0.5-1.0 P.sub.2 O.sub.5 :40-100 H.sub.2 O where "DPA" denotes di-n-propylamine and "q" denotes the oxidation state of chromium.

The reaction mixture is seeded with crystals of AlPO.sub.4 -31 (U.S. Pat. No. 4,310,440) and digested by placing the reaction mixture in a sealed stainless steel pressure vessel and heating it at an effective temperature and for an effective time until crystals of the CAPO-31 product are obtained. Solids are then recovered by filtration, washed with water and dried in air at room temperature.

The CAPO-31 product's chemical analysis shows the CAPO-31 product contains chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, E and F of FIG. 1.

The X-ray powder diffraction pattern of a CAPO-31 product is characterized by the following data:

______________________________________2.theta. d(.ANG.) Relative Intensity______________________________________8.5-8.6 10.40-10.28 m-s20.2-20.3 4.40-4.37 m21.9-22.1 4.06-4.02 w-m22.6-22.7 3.93-3.92 vs31.7-31.8 2.823-2.814 w-m______________________________________

(b) The X-ray powder diffraction pattern for a calcined CAPO-31 is also characterized by the X-ray pattern of part (a).

(c) When the calcined CAPO-31 of part (b) is utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus the measurements are made on a sample after activation at 350.degree. C. in a vacuum. The following data are used in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed*______________________________________O.sub.2 3.46 100 -183 4O.sub.2 3.46 750 -183 6Cyclohexane 6.0 90 24 3Neopentane 6.2 700 24 3H.sub.2 O 2.65 4.3 24 3H.sub.2 O 2.65 20 24 10______________________________________ *typical amount adsorbed The pore diameter of CAPO-31 is greater than about 6.2 .ANG..

EXAMPLE 8

(Preparation of CAPO-34)

(a) CAPO-34 is prepared from a reaction mixture having a composition, expressed in terms of the molar oxide ratios of the components of the reaction mixture, of:

1.0-2.0 TEAOH:0.05-0.2 Cr.sub.2 O.sub.q :0.5-1.0 Al.sub.2 O.sub.3 :0.5-1.0 P.sub.2 O.sub.5 :40-100 H.sub.2 O where "TEAOH" denotes tetraethylammonium hydroxide and "q" denotes the oxidation state of chromium.

The reaction mixture is digested by placing the reaction mixture in a sealed stainless steel pressure vessel and heating it at an effective temperature and for an effective time until crystals of the CAPO-34 product are obtained. Solids are then recovered by filtration, washed with water and dried in air at room temperature.

The CAPO-34 product's chemical analysis shows the CAPO-34 product contains chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, E and F of FIG. 1.

The X-ray powder diffraction pattern of a CAPO-34 product is characterized by the following data:

______________________________________2.theta. d(.ANG.) Relative Intensity______________________________________ 9.4-9.65 9.41-9.17 s-vs15.9-16.2 5.57-5.47 vw-m17.85-18.4 4.97-4.82 w-s20.3-20.9 4.37-4.25 m-vs24.95-25.4 3.57-3.51 vw-s30.3-30.8 2.95-2.90 w-s______________________________________

(b) The X-ray powder diffraction pattern for a calcined CAPO-34 is also characterized by the X-ray pattern of part (a).

(c) When the calcined CAPO-34 of part (b) is utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus the measurements are made on a sample after activation at 350.degree. C. in a vacuum. The following data are used in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed*______________________________________O.sub.2 3.46 100 -183 13O.sub.2 3.46 750 -183 18n-Hexane 4.3 100 24 6H.sub.2 O 2.65 4.3 24 15H.sub.2 O 2.65 20 24 21______________________________________ *typical amount adsorbed

The pore diameter of CAPO-34 is about 4.3 .ANG..

EXAMPLE 9

(Preparation of CAPO-44)

(a) CAPO-44 is prepared from a reaction mixture having a composition, expressed in terms of the molar oxide ratios of the components of the reaction mixture, of:

1.0-2.0 CHA:0.05-0.2 Cr.sub.2 O.sub.q :0.5-1.0 Al.sub.2 O.sub.3 :0.5-1.0 P.sub.2 O.sub.5 :40-100 H.sub.2 O where "CHA" denotes cyclohexylamine and "q" denotes the oxidation state of chromium.

The reaction mixture is digested by placing the reaction mixture in a sealed stainless steel pressure vessel and heating it at an effective temperature and for an effective time until crystals of the CAPO-44 product are obtained. Solids are then recovered by filtration, washed with water and dried in air at room temperature.

The CAPO-44 product's chemical analysis shows the CAPO-44 product contains chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points A, B, C, E and F of FIG. 1.

The X-ray powder diffraction pattern of a CAPO-44 product is characterized by the following data:

______________________________________2.theta. d(.ANG.) Relative Intensity______________________________________ 9.4-9.55 9.41-9.26 vs13.0-13.1 6.81-6.76 w-m16.0-16.2 5.54-5.47 w-m 20.6-20.85 4.31-4.26 s-vs24.3-24.4 3.66-3.65 w-vs 30.7-30.95 2.912-2.889 w-s______________________________________

(b) When the calcined CAPO-44 of part (b) is utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus the measurements are made on a sample after activation at 350.degree. C. in a vacuum. The following data are used in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed*______________________________________O.sub.2 3.46 100 -183 13O.sub.2 3.46 750 -183 16n-Hexane 4.3 100 24 2H.sub.2 O 2.65 4.3 24 15H.sub.2 O 2.65 20 24 17______________________________________ *typical amount adsorbed

The pore diameter of CAPO-44 is about 4.3 .ANG..

EXAMPLE 10

(Preparation of CAPO-18)

An initial mixture was formed by mixing 1.2 grams of a precipitated amorphous chromium phosphate, CrPO.sub.4 (25.7 wt. percent H.sub.2 O), which had been ground with a mortar and pestle, with 5.4 grams of hydrated aluminum oxide in the form of a pseudo-boehmite phase comprising 75.1 wt. percent of Al.sub.2 O.sub.3 and 24.9 wt. percent of H.sub.2 O. This dry mixture was added very slowly (over about 15 minutes) to 9.2 grams of 85 wt. percent orthophosphoric acid (H.sub.3 PO.sub.4) in an ice bath. To the resultant mixture were added 14.7 grams of 40 wt. percent tetraethylammonium hydroxide (TEAOH), and the mixture was mixed until homogeneous. The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

1.0 TEAOH:0.15 CrPO.sub.4 :1.0 Al.sub.2 O.sub.3 :1.00 P.sub.2 O.sub.5 :19.52 H.sub.2 O.

This final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 216 hours. The solid reaction product (which was determined by the analyses described below to be mainly CAPO-18) was recovered by centrifugation, washed with water and dried in air at ambient temperature.

A sample of this solid reaction product was analyzed and the following chemical analysis obtained:

______________________________________Component Weight percent______________________________________Carbon 9.4Cr.sub.2 O.sub.3 2.0Al.sub.2 O.sub.3 33.1P.sub.2 O.sub.5 46.8LOI* 18.4______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.30 TEAOH:0.04 Cr.sub.2 O.sub.3 :1.0 Al.sub.2 O.sub.3 :1.02 P.sub.2 O.sub.5 :0.68 H.sub.a O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.07 TEAOH:(Cr.sub.0.02 Al.sub.0.49 P.sub.0.49)O.sub.2

The product was not pure, but the X-ray powder diffraction pattern of the major phase, as synthesized, was characterized by the data in the following Table FA:

TABLE FA______________________________________(CAPO-18) Relative Intensity2.theta. d(.ANG.) 100 .times. I/I.sub.o______________________________________9.6 9.23 10010.4 8.47 811.0 8.05 1113.1 6.74 614.0 6.32 714.8 5.98 915.5 5.71 2817.0 5.21 6317.9 4.95 2019.2 4.61 519.5 4.54 720.2 4.40 3521.0 4.23 4822.1 4.02 1523.4 3.81 523.9 3.72 524.4 3.64 1224.9 3.57 825.5 3.49 526.1 3.41 1226.5 3.37 726.8 3.32 1128.1 3.18 1229.1 3.07 430.1 2.971 1930.8 2.899 1331.3 2.853 1131.8 2.809 532.5 2.757 2133.5 2.675 534.5 2.596 336.3 2.476 341.9 2.158 343.1 2.100 449.7 1.835 450.0 1.824 451.1 1.786 554.5 1.684 3______________________________________

The X-ray powder diffraction pattern of the major phase, after calcination by heating to 600.degree. C. in air for 1.25 hours, was characterized by the data in the following Table FB:

TABLE FB______________________________________(CAPO-18) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________9.6 9.18 10010.6 8.33 1111.3 7.85 1213.4 6.59 1714.4 6.13 1016.0 5.52 1416.6 5.34 517.2 5.17 2017.4 5.08 1818.4 4.83 519.0 4.66 720.7 4.28 1121.3 4.17 721.5 4.13 821.9 4.06 1622.9 3.88 2824.2 3.67 1124.8 3.58 925.6 3.48 726.3 3.39 727.1 3.28 1527.5 3.24 529.1 3.07 1929.4 3.04 529.8 2.99 430.1 2.969 630.8 2.903 1031.1 2.875 1631.6 2.832 1032.0 2.797 632.5 2.756 533.2 2.700 733.8 2.652 1134.8 2.579 635.4 2.536 637.0 2.427 848.0 1.894 449.8 1.831 550.0 1.824 455.9 1.645 4______________________________________

(b) A sample of the calcined product produced in part (a) was utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus. Before being used in the adsorption tests, the sample was activated by heating to 350.degree. C. overnight in vacuum. The following data was generated in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed______________________________________O.sub.2 3.46 102.5 -183 26.2O.sub.2 3.46 735.0 -183 32.8Neopentane 6.2 102.0 23.0 0.6Neopentane 6.2 748.0 23.2 2.6n-Hexane 4.3 45 23.7 11.5H.sub.2 O 2.65 4.6 24.3 30.9H.sub.2 O 2.65 19.5 23.0 36.8______________________________________

From the above data, the pore size of the calcined product was determined to be greater than 4.3 .ANG., as shown by the adsorption of n-hexane (kinetic diameter of 4.3 .ANG.), but less than 6.2 .ANG., as shown by the negligable adsorption of neopentane (kinetic diameter of 6.2 .ANG.).

Other specimens of CAPO-18 prepared in a similar manner had X-ray powder diffraction patterns similar to those given in Tables FA and FB above. The following general Table FC summarizes the X-ray powder diffraction lines which were obtained from the various specimens of CAPO-18; the least intense lines were not obtained from every specimen.

TABLE FC______________________________________(CAPO-18) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________9.6-9.7 9.11-9.23 10010.4-10.5 8.40-8.48 4-811.0-11.1 7.97-8.05 5-1113.0-13.2 6.69-6.80 3-714.0-14.1 6.28-6.33 3-914.8-14.9 5.95-9.98 4-915.5-15.6 5.66-5.71 17-3017.0-17.1 5.18-5.21 38-6317.9-18.0 4.93-4.96 9-2119.3 4.59-4.61 2-519.5-19.6 4.52-4.54 4-720.2-20.3 4.38-4.40 17-3521.0-21.1 4.20-4.23 25-5822.1-22.2 4.00-4.02 7-1523.4-23.5 3.79-3.81 3-523.9-24.0 3.71-3.72 2-524.4-24.5 3.63-3.64 4-1224.8-25.0 3.56-3.59 3-925.4-25.6 3.48-3.50 4-626.1-26.2 3.40-3.41 8-1226.5-26.7 3.34-3.37 4-726.8-26.9 3.31-3.32 6-1128.1-28.2 3.16-3.18 5-1429.1-29.3 3.05-3.07 3-830.1-30.3 2.954-2.971 10-2830.8-30.9 2.889-2.901 5-1331.3-31.5 2.843-2.853 9-1331.8- 32.0 2.798-2.812 3-632.4-32.6 2.749-2.759 15-2333.5-33.7 2.660-2.675 3-634.5-34.6 2.593-2.596 2-336.2-36.4 2.471-2.479 2-441.8-42.0 2.152-2.160 3-643.0-43.2 2.096-2.105 3-649.7-49.8 1.830-1.835 4-650.0-50.1 1.820-1.824 3-551.1-51.2 1.783-1.788 3-554.5 1.683-1.684 2-3______________________________________

EXAMPLE 11

(Preparation of CAPO-41)

(a) A solution was formed by dissolving 23.2 grams of 85 wt. percent orthophosphoric acid (H.sub.3 PO.sub.4) in 43.2 grams of water. The resultant solution was combined with 13.7 grams of hydrated aluminum oxide in the form of a pseudo-boehmite phase comprising 75.1 wt. percent of Al.sub.2 O.sub.3 and 24.9 wt. percent of H.sub.2 O. Separately, 2.1 grams of chromium acetate hydroxide (Cr.sub.3 (OH).sub.2 (CH.sub.3 COO).sub.7) were dissolved in 40.0 grams of water, and then the resultant solution was added to the previously-prepared mixture. To the resultant mixture were added 10.2 grams of di-n-propylamine (n-Pr.sub.2 NH) and the resultant mixture was mixed until homogeneous. The composition of the final reaction mixture thus produced, expressed in terms of the molar oxide ratios of the components of the reaction mixture, was:

1.0 n-Pr.sub.2 NH:0.1 Cr.sub.2 O.sub.3 :0.9 Al.sub.2 O.sub.3 :1.0 P.sub.2 O.sub.5 :53 H.sub.2 O.

This final reaction mixture was digested by sealing it in a stainless steel pressure vessel lined with polytetrafluoroethylene and heating it in an oven at 200.degree. C. under autogeneous pressure for 48 hours. The solid reaction product (which was determined by the analyses described below to be mainly CAPO-41) was recovered by filtration, washed with water and dried in air at ambient temperature.

A sample of this solid reaction product was analyzed and the following chemical analysis obtained:

______________________________________Component Weight percent______________________________________Carbon 4.3Nitrogen 0.8Cr.sub.2 O.sub.3 2.8Al.sub.2 O.sub.3 35.8P.sub.2 O.sub.5 50.3LOI* 11.1______________________________________ *LOI indicates loss on ignition.

The above chemical analysis corresponds to a product composition of:

0.16 n-Pr.sub.2 NH:0.05 Cr.sub.2 O.sub.3 :1.00 Al.sub.2 O.sub.3 :1.01 P.sub.2 O.sub.5 :0.81 H.sub.2 O, which corresponds to an empirical chemical formula, on an anhydrous basis, of: 0.04 n-Pr.sub.2 NH:(Cr.sub.0.02 Al.sub.0.48 P.sub.0.49)O.sub.2

Microprobe analysis of crystals having the morphology expected for CAPO-41 indicated the following relative proportions of chromium, aluminum and phosphorus:

Cr.sub.0.04 Al.sub.0.43 P.sub.0.53 so that the product contained chromium, aluminum and phosphorus in amounts within the hexagonal compositional area defined by points, A, B, C, D, E and F of FIG. 1.

The product was not pure, but the X-ray powder diffraction pattern of the major phase, as synthesized, was characterized by the data in the following Table RA:

TABLE RA______________________________________(CAPO-41) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________6.8 12.95 269.7 9.11 2113.8 6.43 2718.3 4.85 720.5 4.32 721.2 4.20 10022.3 3.99 7223.0 3.87 2923.3 3.82 2625.3 3.52 1325.9 3.44 1728.1 3.18 329.2 3.06 429.6 3.02 1131.5 2.839 533.6 2.666 536.6 2.454 337.1 2.422 437.8 2.382 1038.4 2.343 543.1 2.098 449.4 1.843 3______________________________________

The X-ray powder diffraction pattern of the major phase, after calcination by heating in air from 100.degree. C. to 500.degree. C. at 100.degree. C. per hour, then heating at 500.degree. C. for a further 1 hour, was characterized by the data in the following Table RB:

TABLE RB______________________________________(CAPO-41) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________6.7 13.12 189.8 9.06 3612.8 6.89 413.6 6.51 2815.9 5.56 420.4 4.36 1021.3 4.16 10022.3 3.98 5423.0 3.86 3025.4 3.51 1725.5 3.49 1625.8 3.45 1028.7 3.11 529.2 3.05 529.5 3.03 829.7 3.01 730.0 2.98 531.6 2.835 438.0 2.369 8______________________________________

(b) A sample of the calcined product produced in part (a) was utilized in adsorption capacity studies using a standard McBain-Bakr gravimetric adsorption apparatus. Before being used in the adsorption tests, the sample was activated by heating to 350.degree. C. overnight in vacuum. The following data was generated in the adsorption studies:

______________________________________ Kinetic Pressure Wt. %Adsorbate Diameter (.ANG.) (Torr) Temp, .degree.C. Adsorbed______________________________________O.sub.2 3.46 102.5 -183 9.9O.sub.2 3.46 735.0 -183 16.2Neopentane 6.2 102.0 23.0 0.8Neopentane 6.2 748.0 23.2 2.5n-Hexane 4.3 45 23.7 4.6H.sub.2 O 2.65 4.6 24.3 11.2H.sub.2 O 2.65 19.5 23.0 24.6______________________________________

From the above data, the pore size of the calcined product was determined to be greater than 4.3 .ANG., as shown by the adsorption of n-hexane (kinetic diameter of 4.3 .ANG.), but less than 6.2 .ANG., as shown by the negligable adsorption of neo-pentane (kinetic diameter of 6.2 .ANG.).

Other specimens of CAPO-41 prepared in a similar manner had X-ray powder diffraction patterns similar to those given in Tables RA and RB above. The following general Table RC summarizes the X-ray powder diffraction lines which were obtained from the various specimens of CAPO-41; the least intense lines were not obtained from every specimen.

TABLE RC______________________________________(CAPO-41) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________6.7-6.9 12.81-12.95 18-389.7-9.8 9.04-9.11 21-3213.8-13.9 6.38-6.43 27-3918.3 4.84-4.85 7-920.5 4.32 7-1121.2-21.3 4.18-4.20 10022.3-22.4 3.97-3.99 72-8723.0 3.87 29-3523.3 3.82 26-3625.3-25.5 3.50-3.52 1325.9-26.0 3.42-3.44 17-2628.1 3.17-3.18 3-829.1-29.2 3.06-3.07 4-529.6-29.7 3.01-3.02 11-1731.5-31.6 2.829-2.839 5-633.6-33.7 2.662-2.666 5-736.6-36.8 2.439-2.454 3-537.1-37.2 2.419-2.422 4-637.8-37.9 2.374-2.382 10-1238.4 2.343-2.345 5-1143.1-43.3 2.091-2.098 4-549.4 1.843-1.844 3-8______________________________________

PROCESS APPLICATIONS

The CAPO compositions of the present invention are, in general, hydrophilic and adsorb water preferentially over common hydrocarbon molecules such as paraffins, olefins and aromatic species, e.g., benzene, xylenes and cumene. Thus the present molecular sieve compositions as a class are useful as desiccants in such adsorption separation/purification processes as natural gas drying, cracked gas drying. Water is also preferentially adsorbed over the so-called permanent gases such as carbon dioxide, nitrogen oxygen and hydrogen. These CAPOs are therefore suitably employed in the drying of reformer hydrogen streams and in the drying of oxygen, nitrogen or air prior to liquifaction.

The present CAPO compositions also exhibit novel surface selectivity characteristics which render them useful as catalyst or catalyst bases in a number of hydrocarbon conversion and oxidative combustion reactions. They can be impregnated or otherwise loaded with catalytically active metals by methods well known in the art (e.g. ion exchange or impregnation) and used, for example, in fabricating catalyst compositions having silica or alumina bases. Of the general class, those species having pores larger than about 4 .ANG. are preferred for catalytic applications.

Among the hydrocarbon conversion reactions catalyzed by CAPO compositions are cracking, hydrocracking, alkylation for both the aromatic and isoparaffin types, isomerization including xylene isomerization, polymerization, reforming, hydrogenation, dehydrogenation, transalkylation, dealkylation, hydrodecyclization and dehydrocyclization.

Using CAPO catalyst compositions which contain a hydrogenation promoter such as platinum or palladium, heavy petroleum residual stocks, cyclic stocks and other hydrocrackable charge stocks, can be hydrocracked at temperatures in the range of 400.degree. F. to 825.degree. F. (204.degree. C. to 441.degree. C.) using molar ratios of hydrogen to hydrocarbon in the range of between 2 and 80, pressures between 10 and 3500 p.s.i.g. (0.171 to 24.23 MPa.), and a liquid hourly space velocity (LHSV) of from 0.1 to 20, preferably 1.0 to 10.

The CAPO catalyst compositions employed in hydrocracking are also suitable for use in reforming processes in which the hydrocarbon feedstocks contact the catalyst at temperatures of from about 700.degree. F. to 1000.degree. F. (371.degree. C. to 538.degree. C.), hydrogen pressures of from 100 to 500 p.s.i.g. (0.791 to 3.448 MPa.), LHSV values in the range of 0.1 to 10 and hydrogen to hydrocarbon molar ratios in the range of 1 to 20, preferably between 4 and 12.

These same catalysts, i.e. those containing hydrogenation promoters, are also useful in hydroisomerization processes in which feedstocks such as normal paraffins are converted to saturated branched chain isomers. Hydroisomerization is carried out at a temperature of from about 200.degree. F. to 600.degree. F. (93.degree. C. to 316.degree. C.), preferably 300.degree. F. to 550.degree. F. (149.degree. C. to 288.degree. C.) with an LHSV value of from about 0.2 to 1.0. Hydrogen (H) is supplied to the reactor in admixture with the hydrocarbon (Hc) feedstock in molar proportions (H/Hc) of between 1 and 5.

At somewhat higher temperatures, i.e. from about 650.degree. F. to 1000.degree. F. (343.degree. C. to 538.degree. C.), preferably 850.degree. F. to 950.degree. F. (454.degree. C. to 510.degree. C.) and usually at somewhat lower pressures within the range of about 15 to 50 p.s.i.g. (205 to 446 KPa.), the same catalyst compositions are used to hydroisomerize normal paraffins. Preferably the paraffin feedstock comprises normal paraffins having a carbon number range of C.sub.7 -C.sub.20. Contact time between the feestock and the catalyst is generally relatively short to avoid undesirable side reactions such as olefin polymerization and paraffin cracking. LHSV values in the range of 0.1 to 10, preferably 1.0 to 6.0 are suitable.

The unique crystal structure of the present CAPO catlysts and their availability in a form totally void of alkali metal content favor their use in the conversion of alkylaromatic compounds, particularly the catalytic disproportionation of toluene, ethylene, trimethyl benzenes, tetramethyl benzenes and the like. In the disproportionation process, isomerization and transalkylation can also occur. Group VIII noble metal adjuvants alone or in conjunction with Group VI-B metals such as tungsten, molybdenum and chromium are preferably included in the catalyst composition in amounts of from about 3 to 15 weight-% of the overall composition. Extraneous hydrogen can, but need not, be present in the reaction zone which is maintained at a temperature of from about 400.degree. to 750.degree. F. (204.degree. to 399.degree. C.), pressures in the range of 100 to 2000 p.s.i.g. (0.791 to 13.89 MPa.) and LHSV values in the range of 0.1 to 15.

Catalytic cracking processes are preferably carried out with CAPO compositions using feedstocks such as gas oils, heavy naphthas, deasphalted crude oil residua, etc., with gasoline being the principal desired product. Temperature conditions of 850.degree. to 1100.degree. F. (454.degree. to 593.degree. C.), LHSV values of 0.5 to 10 and pressure conditions of from about 0 to 50 p.s.i.g. (101 to 446 KPa.) are suitable.

Dehydrocyclization reactions employing paraffinic hydrocarbon feedstocks, preferably normal paraffins having more than 6 carbon atoms, to form benzene, xylenes, toluene and the like are carried out using essentially the same reaction conditions as for caralytic cracking. For these reactions it is preferred to use the CAPO catalyst in conjunction with a Group VIII non-noble metal cation such as cobalt and nickel.

In catalytic dealkylation wherein it is desired to cleave paraffinic side chains from aromatic nuclei without substantially hydrogenating the ring structure, relatively high temperatures in the range of about 800.degree.-1000.degree. F. (427.degree.-538.degree. C.) are employed at moderate hydrogen pressures of about 300-1000 p.s.i.g. (2.17-6.895 MPa.), other conditions being similar to those described above for catalytic hydrocracking. Preferred catalysts are of the same type described above in connection with catalytic dehydrocyclization. Particularly desirable dealkylation reactions contemplated herein include the conversion of methylnaphthalene to naphthalene and toluene and/or xylenes to benzene.

In catalytic hydrofining, the primary objective is to promote the selective hydrodecomposition of organic sulfur and/or nitrogen compounds in the feed, without substantially affecting hydrocarbon molecules therein. For this purpose it is preferred to employ the same general conditions described above for catalytic hydrocracking, and catalysts of the same general nature described in connection with dehydrocyclization operations. Feedstocks include gasoline fractions, kerosenes, jet fuel fractions, diesel fractions, light and heavy gas oils, deasphalted crude oil residua and the like. Any of these may contain up to about 5 weight-percent of sulfur and up to about 3 weight-percent of nitrogen.

Similar conditions can be employed to effect hydrofining, i.e., denitrogenation and desulfurization, of hydrocarbon feeds containing substantial proportions of organonitrogen and organosulfur compounds. It is generally recognized that the presence of substantial amounts of such constituents markedly inhibits the activity of hydrocracking catalysts. Consequently, it is necessary to operate at more extreme conditions when it is desired to obtain the same degree of hydrocracking conversion per pass on a relatively nitrogenous feed than with a feed containing less organonitrogen compounds. Consequently, the conditions under which denitrogenation, desulfurization and/or hydrocracking can be most expeditiously accomplished in any given situation are necessarily determined in view of the characteristics of the feedstocks, in particular the concentration of organonitrogen compounds in the feedstock. As a result of the effect of organonitrogen compounds on the hydrocracking activity of these compositions it is not at all unlikely that the conditions most suitable for denitrogenation of a given feedstock having a relatively high organonitrogen content with minimal hydrocracking, e.g., less than 20 volume percent of fresh feed per pass, might be the same as those preferred for hydrocracking another feestock having a lower concentration of hydrocracking inhibiting constituents, e.g., organonitrogen compounds. Consequently, it has become the practice in this art to establish the conditions under which a certain feed is to be contacted on the basis of preliminary screening tests with the specific catalyst and feedstock.

Isomerization reactions are carried out under conditions similar to those described above for reforming, using somewhat more acidic catalysts. Olefins are preferably isomerized at temperatures of 500.degree.-900.degree. F. (260.degree.-482.degree. C.), while paraffins, naphthenes and alkyl aromatics are isomerized at temperatures of 700.degree.-1000.degree. F. (371.degree.-538.degree. C.). Particularly desirable isomerization reactions contemplated herein include the conversion of n-heptene and/or n-octane to isoheptanes, iso-octanes, butane to iso-butane, methylcyclopentane to cyclohexane, meta-xylene and/or ortho-xylene to paraxylene, 1-butene to 2-butene and/or isobutene, n-hexane to isohexene, cyclohexene to methylcyclopentene etc. The preferred form of the catalyst is a combination of the CAPO with polyvalent metal compounds (such as sulfides) of metals of Group II-A, Group II-B and rare earth metals. For alkylation and dealkylation processes the CAPO compositions having pores of at least 5 .ANG. are preferred. When employed for dealkylation of alkyl aromatics, the temperature is usually at least 350.degree. F. (177.degree. C.) and ranges up to a temperature at which substantial cracking of the feedstock or conversion products occurs, generally up to about 700.degree. F. (371.degree. C.). The temperature is preferably at least 450.degree. F. (232.degree. C.) and not greater than the critical temperature of the compound undergoing dealkylation. Pressure conditions are applied to retain at least the aromatic feed in the liquid state. For alkylation the temperature can be as low as 250.degree. F. (121.degree. C.) but is preferably at least 350.degree. F. (177.degree. C.). In the alkylation of benzene, toluene and xylene, the preferred alkylating agents are olefins such as ethylene and propylene.

The following examples are provided to further illustrate the use of the CAPOs of the invention in certain of the processes discussed above, but are not intended to be limitative of the possible uses of the CAPOs.

EXAMPLE 12

(Cracking tests on CAPO-5)

The n-butane cracking activity of the calcined CAPO-5 prepared in Example 2 above was tested in a bench-scale apparatus, in which the reactor was a cylindrical quartz tube 254 mm. in length and 10.3 mm. in internal diameter. The reactor was loaded with 0.67 gram of the calcined CAPO-5 and a feedstock comprising a helium/n-butane mixture containing 2 mole percent of n-butane was then passed through the reactor at a rate of 50 mL/min. (STP) at 500.degree. C. for 50 minutes. At the end of this period, the reactor effluent was analyzed using conventional gas chromatography techniques. The resultant data showed a pseudo-first-order rate constant (k.sub.A) of 2.1.

EXAMPLE 13

(Cracking tests on CAPO-41)

The n-butane cracking activity of the calcined CAPO-41 prepared in Example 11 above was tested in the same way as in Example 12 above, except that the weight of the calcined material in the reactor was 2.00 gram and that the measurements were taken after the helium/n-butane mixture had been flowing for 10 minutes. The resultant data showed a pseudo-first-order rate constant (k.sub.A) of 2.3.

Claims

1. Crystalline molecular sieves having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of -1 or +1, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1, said crystalline molecular sieves having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in one of the following Tables A to H and J to V;

TABLE A______________________________________(CAPO-5)2.theta. d(.ANG.) Relative Intensity______________________________________ 7.3-7.65 12.1-11.56 m-vs19.5-20.0 4.55-4.44 m-s20.9-21.3 4.25-4.17 m-vs22.2-22.6 4.00-3.93 w-vs25.7-26.2 3.47-3.39 w-m______________________________________

TABLE B______________________________________(CAPO-11)2.theta. d(.ANG.) Relative Intensity______________________________________ 9.3-9.65 9.51-9.17 m-s20.2-20.6 4.40-4.31 m-s20.9-21.3 4.25-4.17 s-vs22.0-22.5 4.04-3.95 m-s22.5-22.9 3.95-3.92 m-s23.0-23.4 3.87-3.80 m-vs______________________________________

TABLE C______________________________________(CAPO-14)2.theta. d(.ANG.) Relative Intensity______________________________________8.6-8.9 10.3-9.93 vs13.0 6.81 w21.9-22.2 4.06-4.00 w25.4 3.51 w27.5 3.24 w29.7 3.01 w______________________________________

TABLE D______________________________________(CAPO-16)2.theta. d(.ANG.) Relative Intensity______________________________________11.3-11.6 7.83-7.63 m-vs18.7-18.9 4.75-4.70 w-s21.9-22.3 4.06-3.99 m-vs26.5-27.0 3.363-3.302 w-m 29.7-30.05 3.008-2.974 w-m______________________________________

TABLE E______________________________________(CAPO-17)2.theta. d(.ANG.) Relative Intensity______________________________________ 7.7-7.75 11.5-11.4 vs13.4 6.61 s-vs 15.5-15.55 5.72-5.70 s19.65-19.7 4.52-4.51 w-s20.5-20.6 4.33-4.31 vs 31.8-32.00 2.812-2.797 w-s______________________________________

TABLE F______________________________________(CAPO-18)2.theta. d(.ANG.) Relative Intensity______________________________________9.5-9.7 9.23-9.16 vs15.4-15.6 5.76-5.66 m16.9-17.1 5.25-5.19 m20.15-20.3 4.41-4.38 m20.95-21.1 4.24-4.20 m31.8-32.6 2.814-2.749 m______________________________________

TABLE G______________________________________(CAPO-20)2.theta. d(.ANG.) Relative Intensity______________________________________ 13.7-14.25 6.46-6.22 m-vs19.55-20.0 4.54-4.44 w-s24.05-24.5 3.70-3.63 m-vs34.3-35.0 2.614-2.564 vw-w42.5-43.0 2.127-2.103 vw-w______________________________________

TABLE H______________________________________(CAPO-31)2.theta. d(.ANG.) Relative Intensity______________________________________8.5-8.6 10.40-10.28 m-s20.2-20.3 4.40-4.37 m21.9-22.1 4.06-4.02 w-m22.6-22.7 3.93-3.92 vs31.7-31.8 2.823-2.814 w-m______________________________________

TABLE J*______________________________________(CAPO-33)2.theta. d(.ANG.) Relative Intensity______________________________________9.25-9.55 9.56-9.26 w-m12.5-12.9 7.08-6.86 vs16.9-17.3 5.25-5.13 w-m20.45-20.9 4.34-4.25 w-m23.85-24.25 3.73-3.67 w-m26.05-26.35 3.42-3.38 w-m27.3-27.6 3.27-3.23 vs______________________________________ *as-synthesized form

TABLE K*______________________________________(CAPO-33)2.theta. d(.ANG.) Relative Intensity______________________________________13.15-13.4 6.73-6.61 vs18.05-18.35 4.91-4.83 m18.4-18.6 4.82-4.77 m26.55-26.7 3.36-3.34 m32.0-32.1 2.80-2.79 m______________________________________ *calcined form

TABLE L______________________________________(CAPO-34)2.theta. d(.ANG.) Relative Intensity______________________________________ 9.4-9.65 9.41-9.17 s-vs15.9-16.2 5.57-5.47 vw-m17.85-18.4 4.97-4.82 w-s20.3-20.9 4.37-4.25 m-vs24.95-25.4 3.57-3.51 vw-s30.3-30.8 2.95-2.90 w-s______________________________________

TABLE M______________________________________(CAPO-35)2.theta. d(.ANG.) Relative Intensity______________________________________10.8-11.1 8.19-7.97 m17.2-17.4 5.16-5.10 s-vs 21.0-21.25 4.23-4.18 m-s21.8-22.0 4.08-4.04 vs31.8-32.2 2.814-2.788 m______________________________________

TABLE N______________________________________(CAPO-36)2.theta. d(.ANG.) Relative Intensity______________________________________7.7-7.9 11.5-11.2 vs16.2-16.6 5.47-5.34 w-m18.9-19.3 4.70-4.60 m-s20.6-20.8 4.31-4.27 w-s21.8-22.0 4.08-4.04 m22.2-22.5 4.00-3.95 w-m______________________________________

TABLE O______________________________________(CAPO-37)2.theta. d(.ANG.) Relative Intensity______________________________________6.1-6.3 14.49-14.03 vs15.5-15.7 5.72-5.64 w-m18.5-18.8 4.80-4.72 w-m23.5-23.7 3.79-3.75 w-m26.9-27.1 3.31-3.29 w-m______________________________________

TABLE P______________________________________(CAPO-39)2.theta. d(.ANG.) Relative Intensity______________________________________9.4-9.6 9.41-9.21 w-m13.3-13.6 6.66-6.51 m-vs18.0-18.4 4.93-4.82 m21.2-21.5 4.19-4.13 m-s22.5-23.0 3.95-3.87 s-vs30.2-30.5 2.96-2.93 w-m______________________________________

TABLE Q______________________________________(CAPO-40)2.theta. d(.ANG.) Relative Intensity______________________________________7.5-7.7 11.79-11.48 vw-m8.0-8.1 11.05-10.94 s-vs12.4-12.5 7.14-7.08 w-vs13.6-13.8 6.51-6.42 m-s14.0-14.1 6.33-6.28 w-m27.8-28.0 3.209-3.187 w-m______________________________________

TABLE R______________________________________(CAPO-41)2.theta. d(.ANG.) Relative Intensity______________________________________13.6-13.9 6.51-6.38 w-m21.1-21.3 4.21-4.17 vs22.1-22.4 4.02-3.97 m-s23.0-23.4 3.87-3.80 w-m25.5-26.0 3.493-3.440 w-m______________________________________

TABLE S______________________________________(CAPO-42)2.theta. d(.ANG.) Relative Intensity______________________________________7.15-7.4 12.36-11.95 m-vs12.5-12.7 7.08-6.97 m-s21.75-21.9 4.09-4.06 m-s 24.1-24.25 3.69-3.67 vs27.25-27.4 3.273-3.255 s30.05-30.25 2.974-2.955 m-s______________________________________

TABLE T______________________________________(CAPO-44)2.theta. d(.ANG.) Relative Intensity______________________________________ 9.4-9.55 9.41-9.26 vs13.0-13.1 6.81-6.76 w-m16.0-16.2 5.54-5.47 w-m 20.6-20.85 4.31-4.26 s-vs24.3-24.4 3.66-3.65 w-vs 30.7-30.95 2.912-2.889 w-s______________________________________

TABLE U______________________________________(CAPO-46)2.theta. d(.ANG.) Relative Intensity______________________________________7.2-8.1 12.3-10.9 vs21.2-21.8 4.19-4.08 w-m22.5-23.0 3.95-3.87 vw-m26.6-27.2 3.351-3.278 vw-w28.5-29.0 3.132-3.079 vw-w______________________________________

TABLE V______________________________________(CAPO-47)2.theta. d(.ANG.) Relative Intensity______________________________________9.4 9.41 vs15.9-16.0 5.57-5.54 w-m20.5-20.6 4.33-4.31 s24.5-24.7 3.63-3.60 w25.8-25.9 3.45-3.44 w30.4-30.5 2.940-2.931 w.______________________________________

2. Crystalline molecular sieves having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of zero, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the pentagonal compositional area defined by points G, H, I, J and K of FIG. 2, said crystalline molecular sieves having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in one of Tables A to H and J to V in claim 1.

3. Molecular sieves according to claim 1 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the tetragonal compositional area defined by points a, b, c and d of FIG. 3.

4. Molecular sieves according to claim 3 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the hexagonal compositional area defined by points, n, o, p, q, r and s of FIG. 3.

5. Molecular sieves according to claim 2 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the pentagonal compositional area defined by points e, f, g, h and i of FIG. 4.

6. Molecular sieves according to claim 1 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the tetragonal compositional area defined by points j, k, l and m of FIG. 5.

7. Molecular sieves according to claim 1 wherein "m" is not greater than about 0.15.

8. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacing set forth in Table A given in claim 1.

9. The crystalline molecular sieves of claim 8 wherein the X-ray powder diffraction pattern set forth in Table A contains at least the d-spacings set forth in the following Table AA:

TABLE AA______________________________________(CAPO-5) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________7.4 11.89 10012.9 6.84 815.0 5.92 2019.8 4.47 4421.0 4.23 4722.5 3.95 6424.8 3.59 326.1 3.41 2129.1 3.07 930.2 2.956 1233.8 2.656 434.8 2.580 1037.1 2.421 337.8 2.382 941.8 2.159 248.0 1.893 3.______________________________________

10. The crystalline molecular sieves of claim 8 wherein the X-ray powder diffraction pattern set forth in Table A contains at least the d-spacings set forth in the following Table AB:

TABLE AB______________________________________(CAPO-5) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________7.5 11.83 10013.0 6.83 2119.9 4.47 2221.2 4.19 4522.5 3.94 6324.9 3.57 326.1 3.42 2029.2 3.06 1630.2 2.963 1233.9 2.645 434.7 2.587 1038.0 2.368 6.______________________________________

11. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table B given in claim 1.

12. The crystalline molecular sieves of claim 11 wherein the X-ray powder diffraction pattern set forth in Table B contains at least the d-spacings set forth in the following Table BA:

TABLE BA______________________________________(CAPO-11) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________8.1 10.91 239.4 9.36 6613.2 6.70 1115.7 5.65 2716.3 5.43 419.0 4.66 620.5 4.34 3021.0 4.22 10022.2 4.01 4722.6 3.94 4422.7 3.91 4723.2 3.83 5524.7 3.60 726.4 3.38 1126.6 3.34 1128.7 3.11 1429.6 3.02 631.5 2.837 733.0 2.718 1034.3 2.616 736.6 2.456 337.6 2.389 837.9 2.376 1242.8 2.111 445.1 2.010 349.0 1.860 350.8 1.798 3.______________________________________

13. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table C given in claim 1.

14. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table D given in claim 1.

15. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table E given in claim 1.

16. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table F given in claim 1.

17. The crystalline molecular sieves of claim 16 wherein the X-ray powder diffraction pattern set forth in Table F contains at least the d-spacings set forth in one of the following Tables FA and FB:

TABLE FA______________________________________(CAPO-18) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________9.6 9.23 10010.4 8.47 811.0 8.05 1113.1 6.74 614.0 6.32 714.8 5.98 915.5 5.71 2817.0 5.21 6317.9 4.95 2019.2 4.61 519.5 4.54 720.2 4.40 3521.0 4.23 4822.1 4.02 1523.4 3.81 523.9 3.72 524.4 3.64 1224.9 3.57 825.5 3.49 526.1 3.41 1226.5 3.37 726.8 3.32 1128.1 3.18 1229.1 3.07 430.1 2.971 1930.8 2.899 1331.3 2.853 1131.8 2.809 532.5 2.757 2133.5 2.675 534.5 2.596 336.3 2.476 341.9 2.158 343.1 2.100 449.7 1.835 450.0 1.824 451.1 1.786 554.5 1.684 3______________________________________

TABLE FB______________________________________(CAPO-18) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________9.6 9.18 10010.6 8.33 1111.3 7.85 1213.4 6.59 1714.4 6.13 1016.0 5.52 1416.6 5.34 517.2 5.17 2017.4 5.08 1818.4 4.83 519.0 4.66 720.7 4.28 1121.3 4.17 721.5 4.13 821.9 4.06 1622.9 3.88 2824.2 3.67 1124.8 3.58 925.6 3.48 726.3 3.39 727.1 3.28 1527.5 3.24 529.1 3.07 1929.4 3.04 529.8 2.99 430.1 2.969 630.8 2.903 1031.1 2.875 1631.6 2.832 1032.0 2.797 632.5 2.756 533.2 2.700 733.8 2.652 1134.8 2.579 635.4 2.536 637.0 2.427 848.0 1.894 449.8 1.831 550.0 1.824 455.9 1.645 4.______________________________________

18. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table G given in claim 1.

19. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table H given in claim 1.

20. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table J given in claim 1.

21. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table K given in claim 1.

22. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table L given in claim 1.

23. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table M given in claim 1.

24. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table N given in claim 1.

25. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table O given in claim 1.

26. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table P given in claim 1.

27. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table Q given in claim 1.

28. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table R given in claim 1.

29. The crystalline molecular sieves of claim 28 wherein the X-ray powder diffraction pattern set forth in Table R contains at least the d-spacings set forth in one of the following Tables RA and RB:

TABLE RA______________________________________(CAPO-41) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________6.8 12.95 269.7 9.11 2113.8 6.43 2718.3 4.85 720.5 4.32 721.2 4.20 10022.3 3.99 7223.0 3.87 2923.3 3.82 2625.3 3.52 1325.9 3.44 1728.1 3.18 329.2 3.06 429.6 3.02 1131.5 2.839 533.6 2.666 536.6 2.454 337.1 2.422 437.8 2.382 1038.4 2.343 543.1 2.098 449.4 1.843 3______________________________________

TABLE RB______________________________________(CAPO-41) Relative Intensity2.theta. d (.ANG.) 100 .times. I/I.sub.o______________________________________6.7 13.12 189.8 9.06 3612.8 6.89 413.6 6.51 2815.9 5.56 420.4 4.36 1021.3 4.16 10022.3 3.98 5423.0 3.86 3025.4 3.51 1725.5 3.49 1625.8 3.45 1028.7 3.11 529.2 3.05 529.5 3.03 829.7 3.01 730.0 2.98 531.6 2.835 438.0 2.369 8.______________________________________

30. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table S given in claim 1.

31. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table T given in claim 1.

32. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table U given in claim 1.

33. The crystalline molecular sieves of claim 1 or 2 having a characteristic X-ray powder diffraction pattern which contains at least the d-spacings set forth in Table V given in claim 1.

34. Crystalline molecular sieves having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of -1 or +1, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1.

35. Crystalline molecular sieves having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of zero, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the pentagonal compositional area defined by points G, H, I, J and K of FIG. 2.

36. Molecular sieves according to claim 34 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the tetragonal compositional area defined by points a, b, c and d of FIG. 3.

37. Molecular sieves according to claim 36 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the hexagonal compositional area defined by points n, o, p, q, r and s of FIG. 3.

38. Molecular sieves according to claim 35 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the pentagonal compositional area defined by points e, f, g, h and i of FIG. 4.

39. Moleculae sieves according to claim 34 wherein the mole fractions of chromium, aluminum and phosphorus present as tetrahedral oxides are within the tetragonal compositional area defined by points j, k, l and m of FIG. 5.

40. Molecular sieves according to claim 34 wherein "m" is not greater than about 0.15.

41. Process for preparing crystalline molecular sieves having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of -1 or +1, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1, which comprises providing a reation mixture composition at an effective temperature and for an effective time sufficient to produce said molecular sieves, said reaction mixture composition being expressed in terms of molar oxide ratios as follows:

aR:(Cr.sub.u Al.sub.v P.sub.w)O.sub.2 :bH.sub.2 O

wherein "R" is an organic templating agent; "a" is an effective amount of "R" greater than zero; "b" has a value of from zero to about 500; and "u", "v" and "w" represent the mole fractions, respectively, of chromium, aluminum and phosphorus in the (Cr.sub.u Al.sub.v P.sub.w)O.sub.2 constituent, and each has a value of at least 0.01.

42. The process of claim 41 wherein "u", "v" and "w" are within the pentagonal compositional area defined by points L, M, N, O and P of FIG. 6.

43. The process of claim 41 wherein "a" is not greater than about 0.6.

44. The process of claim 41 wherein "b" is not greater than about 20.

45. Process according to claim 42 wherein the reaction mixture composition comprises from about 0.1 to about 0.4 moles of chromium per mole of phosphorus.

46. Process according to claim 41 wherein the reaction mixture composition comprises from about 0.75 to about 1.25 moles of aluminum per mole of phosphorus.

47. Process according to claim 41 wherein the source of phosphorus in the reaction mixture is orthophosphoric acid.

48. Process according to claim 47 wherein the source of phosphorus in the reaction mixture is orthophosphoric acid and the source of aluminum is at least one compound selected from the group consisting of pseudo-boehmite, aluminum chlorhydrol and aluminum alkoxides.

49. Process according to claim 48 wherein the aluminum alkoxide is aluminum isopropoxide.

50. Process according to claim 41 wherein the source of chromium is selected from the group consisting of oxides, alkoxides, hydroxides, chlorides, bromides, iodides, nitrates, sulfates, carboxylates and mixtures thereof.

51. Process according to claim 41 wherein the source of chromium is chromium(III) orthophosphate, chromium(III) acetate or chromium acetate hydroxide.

52. Process according to claim 41 wherein the organic templating agent is a quaternary ammonium or quaternary phosphonium compound having the formula:

R.sub.4 X.sup.+

wherein X is nitrogen or phosphorus and each R is an alkyl or aryl group containing from 1 to 8 carbon atoms.

53. Process according to claim 41 wherein the organic templating agent is an amine.

54. Process according to claim 41 wherein the templating agent is selected from the group consisting of tetrapropylammonium ion; tetraethylammonium ion; tripropylamine; triethylamine; triethanolamine; piperidine; cyclohexylamine; 2-methyl pyridine; N,N-dimethylbenzylamine; N,N-dimethylethanolamine; choline; N,N-dimethylpiperzine; 1,4-diaziabicyclo-(2,2,2)octane; N-methyldiethanolamine; N-methylethanolamine; N-methylpipereidine; 3-methylpiperidine; N-methylcyclohexylamine; 3-methylpyridine; 4-methylpyridine; quinuclidine; N,N'-dimethyl-1,4-diazabicyclo(2,2,2)octane ion; tetramethylammonium ion; tetrabutylammonium ion; tetrapentylammonium ion; di-n-butylamine; neopentylamine; di-n-pentylamine; isopropylamine; t-butylamine; ethylenediamine; pyrrolidine; 2-imidazolidone; di-n-propylamine; and a polymeric quaternary ammonium salt [(C.sub.14 H.sub.32 N.sub.2)(OH).sub.2 ].sub.x wherein x has a value of at least 2.

55. Molecular sieve prepared by calcining, at a temperature sufficiently high to remove at some of any organic templating agent pressure in the intracrystalline pore system, a crystalline molecular sieve having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of -1 or +1, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that, they are within the hexagonal compositional area defined by points A, B, C, D, E and F of FIG. 1.

56. Process for preparing crystalline molecular sieves having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of zero, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the pentagonal compositional area defined by points G, H, I, J and K of FIG. 2, which comprises providing a reaction mixture composition at an effective temperature and for an effective time sufficient to produce said molecular sieves, said reaction mixture composition being expressed in terms of molar oxide ratios as follows:

aR:(Cr.sub.u Al.sub.v P.sub.w)O.sub.2 :bH.sub.2 O

wherein "R" is an organic templating agent; "a" is an effective amount of "R" greater than zero; "b" has a value of from zero to about 500; and "u", "v" and "w" represent the mole fractions, respectively, of chromium, aluminum and phosphorus in the (Cr.sub.u Al.sub.v P.sub.w)O.sub.2 constituent, and each has a value of at least 0.01.

57. The process of claim 56 wherein "u", "v" and "w" are within the pentagonal compositional area defined by points L, M, N, O and P of FIG. 6.

58. The process of claim 56 wherein "a" is not greater than about 0.6.

59. The process of claim 56 wherein "b" is not greater than about 20.

60. Process according to claim 56 wherein the reaction mixture composition comprises from about 0.1 to about 0.4 moles of chromium per mole of phosphorus.

61. Process according to claim 56 wherein the reaction mixture composition comprises from about 0.75 to about 1.25 moles of aluminum per mole of phosphorus.

62. Process according to claim 56 wherein the source of phosphorus in the reaction mixture is orthophosphoric acid.

63. Process according to claim 61 wherein the source of phosphorus in the reaction mixture is orthophosphoric acid and the source of aluminum is at least one compound selected from the group consisting of pseudo-boehmite, aluminum chlorhydrol and aluminum alkoxides.

64. Process according to claim 63 wherein the aluminum alkoxide is aluminum isopropoxide.

65. Process according to claim 56 wherein the source of chromium is selected from the group consisting of oxides, alkoxides, hydroxides, chlorides, bromides, iodides, nitrates, sulfates, carboxylates and mixtures thereof.

66. Process according to claim 56 wherein the organic templating agent is a quaternary ammonium or quaternary phosphonium compound having the formula:

R.sub.4 X.sup.+

wherein X is nitrogen or phosphorus and each R is an alkyl or aryl group containing from 1 to 8 carbon atoms.

67. Process according to claim 56 wherein the organic templating agent is an amine.

68. Process according to claim 56 wherein the templating agent is selected from the group consisting of tetrapropylammonium ion; tetraethylammonium ion; tripropylamine; triethylamine; triethanolamine; piperidine; cyclohexylamine; 2-methyl pyridine; N,N-dimethylbenzylamine; N,N-dimethylethanolamine; choline; N,N-dimethylpiperazine; 1,4-diaziabicyclo-(2,2,2)octane; N-methyldiethanolamine; N-methylethanolamine; N-methylpiperidine; 3-methylpiperidine; N-methylcyclohexylamine; 3-methylpyridine; 4-methylpyridine; quinuclidine; N,N'-dimethyl-1,4-diazabicyclo(2,2,2)octane ion; tetramethylammonium ion; tetrabutylammonium ion; tetrapentylammonium ion; di-n-butylamine; neopentylamine; di-n-pentylamine; isopropylamine; t-butylamine; ethylenediamine; pyrrolidine; 2-imidazolidone; di-n-propylamine; and a polymeric quaternary ammonium salt [(C.sub.14 H.sub.32 N.sub.2)(OH).sub.2 ].sub.x wherein x has a value of at least 2.

69. Molecular sieve prepared by calcining, at a temperature sufficiently high to remove at some of any organic templating agent present in the intracrystalline pore system, a crystalline molecular sieve having three-dimensional microporous framework structures of CrO.sub.2.sup.n, AlO.sub.2 and PO.sub.2 tetrahedral units, where "n" has a value of zero, having an empirical chemical composition on an anhydrous basis expressed by the formula:

mR:(Cr.sub.x Al.sub.y P.sub.z)O.sub.2

wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present pore mole of (Cr.sub.x Al.sub.y P.sub.z)O.sub.2 and has a value of from zero to about 0.3; and "x", "y" and "z" represent the mole fractions of chromium, aluminum and phosphorus, respectively, present as tetrahedral oxides, said mole fractions being such that they are within the pentagonal compositional area defined by points G, H, I, J and K of FIG. 2.