Method for the production of a zeolite material

Abstract

Method for production of a zeolitic material represented by the formula:R.sub.x H.sub.5.sub.-x (Al.sub.y Fe.sub.1.sub.-y).sub.4 (P.sub.l As.sub.1.sub.-l).sub.3 O.sub.16.zH.sub.2 Owherein R represents Na or K, x, y, z and l are numerical values of O.ltoreq.x.ltoreq.5, O.ltoreq.y.ltoreq.1, Z.ltoreq.9 and O.ltoreq.l.ltoreq.1, respectively; which comprises preparing an aqueous solution by dissolving (1) at least one source of aluminum and iron, (2) at least one source of phosphorus and arsenic and (3) at least one source of sodium and potassium in water in the ranges expressed in terms of the molar ratios of their oxides of3.5.ltoreq.(Al, Fe).sub. 2 O.sub.3 /(P, As).sub. 2 O.sub.5 .ltoreq.4.5and(K, Na).sub.2 O/(Al, Fe) .sub.2 O.sub.3 >0.12adjusting the pH of the solution to within the range of the cross-hatched area in FIGS. 1 to 4 and heating the solution at 150 to 250.degree.C in a closed vessel to crystallize the zeolitic material and recovering the objective zeolitic material. The aforementioned zeolitic material is useful for recovering metallic cations from an aqueous solution containing such metallic cations.

Description

This invention relates to a method for recovery of metallic cations utilizing particular zeolitic materials composed of alumino/ferro-phosphate/arsenate.

The recovery of metallic cations by the use of cation exchange membranes has heretofore been known, of which mechanisms are illustrated as the following:

A.sup.+[R]- + B.sup.+(aq) + C.sup.+(aq) .revreaction. B.sup.+[R]- + A.sup.+(aq)+C+(aq) B.sup.+[R].sup.- + H.sup.+(aq) .revreaction. H.sup.+[R].sup.- + B.sup.+(aq) Wherein A.sup.+ stands for a cation contained in the membrane, B.sup.+ stands for a metallic cation to be recovered in an aqueous solution, C.sup.+ stands for a cation co-existing in the aqueous solution, [R].sup.- stands for an anion framework of the membrane. The cation exchange reactions depend on such factors as a cation selectivity in the membranes, the concentration of cations and the temperature of exchange reactions, etc. The lower the cation selectivity in the membranes, the higher the concentration of cation to be removed in an aqueous solution and the higher the temperature, the more the cation exchange reaction is accelerated.

Therefore, for recovering solely desirable metallic cations, it is advantageous that the metallic cation exchanged membranes are washed with a strong acid at a high temperature.

Certain cation exchange resins have been used for recovery of metallic cations. However, these resins have some drawbacks. For example, when a solution containing metallic cations to be recovered has a pH below 3, these resins are not capable of exchanging any metallic cation because of their firm incorporation with proton and, additionally, though the cation exchange reaction is accelerated the reaction temperature is elevated, the cation exchange capacity of these resins is gradually lowered as the temperature is elevated.

Also, it is commonly known that zeolites, e.g. zeolite type A (Linde Company) have cation exchange properties.

However, as the zeolites exhibit a basic character, a metallic cation cannot be eluted with an acidic solution, for example, zeolite type A is easily decomposed with a solution having pH below 5. Therefore, they cannot be used for recovery of metallic cations with acid.

Extensive study has been done to discover the zeolitic materials which are stable against a strong acid and have cation exchange selectivity to Ag.sup.+, Tl.sup.+, Cs.sup.+ and Rb.sup.+ in an aqueous solvent, even under the conditions having pH below about 3 and even at a high temperature of above 100.degree.C.

An object of the present invention is to provide a method for recovery of metallic cations as an acid solution containing solely desirable metallic cations by the use of the particular zeolitic material described below. More particularly, it is to provide a method of recovering Ag.sup.+ as its acid solution from a waste liquor in the photographic porcesses which contains silver as complex cations unexchangeable with the zeolitic material as they are, but contains silver as Ag.sup.+ exchangeable when the pH of the liquor is shifted to below about 4.

The above object can be realized by this invention which comprises contacting a zeolitic material represented by the formula:

M.sub.x H.sub.5.sub.-x [(Al.sub.y Fe.sub.1.sub.-y).sub.4 (P.sub.l As.sub.1.sub.-l).sub.3 O.sub.16 ].zH.sub.2 O (I), the zeolitic material being referred to as "zeolite OTW" hereinafter, wherein M represents a univalent or a one-half bivalent cation and x, y, z and l are numerical values of 0 .ltoreq. x .ltoreq. 5; 0 .ltoreq. y .ltoreq. 1; z .ltoreq. 9 and 0 .ltoreq. l .ltoreq. 1, respectively, with a solution containing metallic cations which are desired to be recovered, whereby the cations represented by M may be exchanged by the desired metallic cation, and then, washing the zeolite OTW with an acid to recover the desired metallic cation so exchanged.

Examples of univalent or one-half bivalent cations represented by M in the above general formula of zeolite OTW used in this invention include H.sup.+, NH.sub.4 .sup.+, Li.sup.+, Na.sup.+, K.sup.+, Rb.sup.+, Cs.sup.+, Ag.sup.+, Tl.sup.+, 1/2Mg.sup.+.sup.+, 1/2Ca.sup.+.sup.+, 1/2Sr.sup.+.sup.+, 1/2Ba.sup.+.sup.+, 1/2Pb.sup.+.sup.+, 1/2Mn.sup.+.sup.+, 1/2Co.sup.+.sup.+, 1/2Cu.sup.+.sup.+, 1/2Ni.sup.+.sup.+, 1/2Fe.sup.+.sup.+ and the like. Although the kind of cations to be employed depends on the kind of metallic cation to be recovered, H.sup.+, K.sup.+, Na.sup.+ and Ca.sup.+.sup.+ can usually be employed to advantage.

The order of selectivity in this zeolite OTW is as follows:

Ag.sup.+, Tl.sup.+>Rb.sup.+, Cs.sup.+>H.sup.+, 1/2Mg.sup.+.sup.+, 1/2Co.sup.+.sup.+, 1/2Cu.sup.+.sup.+, 1/2Ni.sup.+.sup.+, 1/2Fe.sup.+.sup.+, 1/2 Mn.sup.+.sup.+>1/2Ca.sup.+.sup.+, 1/2Sr.sup.+.sup.+, 1/2Ba.sup.+.sup.+>Na.sup.+, K.sup.+, Li.sup.+.

The following test data will support the above fact.

Test

One liter of a solution of about pH 4.5 containing large portions of Na.sup.+ and small proportions each of Tl.sup.+, Ag.sup.+, Cs.sup.+, Rb.sup.+ and Ba.sup.+.sup.+ was heated on a hot water bath, followed by the addition of 0.01 mole of zeolite OTW of formula K.sub.1.5 H.sub.3.5 Fe.sub.4 As.sub.3 O.sub.16.7H.sub.2 O. The mixture was heated for a further 15 minutes. Then, the zeolite OTW was recovered by filtration and washed with four 50 ml. portions of a hot 2N-nitric acid. The washings were combined, concentrated and analyzed. The results are as follows:

______________________________________Original solution Recovered solutionKind of Recoveredcation Mole Percent (%) salt Mole Percent (%)______________________________________Na.sup.+ 0.44 88.5 NaNO.sub.3 0.0002 1.2Ag.sup.+ 0.009 1.8 AgNO.sub.3 0.0062 37.8Cs.sup.+ 0.01 2.0 CsNO.sub.3 0.0033 20.1Rb.sup.+ 0.01 2.0 RbNO.sub.3 0.0033 20.1Tl.sup.+ 0.008 1.6 TlNO.sub.3 0.0024 14.6Ba.sup.+.sup.+ 0.021 4.2 Ba(NO.sub.3).sub.2 0.0010 6.1______________________________________

In the process of this invention, the cation exchange reaction may be conducted at a temperature of 0.degree. to about 250.degree.C, desirably about 50.degree. to about 100.degree.C.

The suitable pH of the solution to be contacted to the zeolite OTW is within the range of about 0 to about 12, desirably about 0.5 to about 9.

The acid to be employed in the washing cycle may be any of sulfuric acid, hydrochloric acid, nitric acid, acetic acid and the like. As a rule, when use is made of e.g. nitric acid or hydrochloric acid, the molecular skeleton of the zeolite OTW is not destroyed even by heating to 50.degree.C in a 4N-acid solution, or by heating to 100.degree.C in a 2N-acid solution. In general, pH of the acids is desirably below about 0.5.

Taking the case of the process for recovering Ag.sup.+, the reaction mechanisms of this invention will be described in detail as follows:

Na.sub.x (Z--OTW)+kAg.sup.+ = Ag.sub.x (Z--OTW)+(k-x)Ag.sup.++xNa.sup.+ (1) Ag.sub.x (Z--OTW)+nHNO.sub.3 = h.sub.x (Z--OTW)+ xAgNO.sub.3 + (n-x)HNO.sub.3 ( 2)

then, by filtering off the H.sub.x (Z--OTW) formed according to formula (2), Ag.sup.+ is recovered as a solution of AgNO.sub.3 in nitric acid.

The concentration process of Ag.sup.+ in a solution containing Ag.sup.+ and Na.sup.+, for example, can be written as follows:

K.sub.x (Z--OTW) + sAg.sup.+ + tNa.sup.+ = (Ag.sub.h Na.sub.x.sub.-h)(Z--OTW)+(s--h)Ag.sup.++(t-x+h)Na.sup.++xK.sup.+(3) (ag.sub.h Na.sub.x.sub.-h)(Z--OTW) + nHNO.sub.3 h.sub.x (Z--OTW) + hAgNO.sub.3 +(x-h)NaNO.sub.3 + (n-x)H.sub.2 O(4)

in the above chemical equation, (Z--OTW) represents H.sub.5.sub.-x [(Al.sub.y Fe.sub.1.sub.-y).sub.4 (P.sub.l As.sub.1.sub.-l).sub.3 O.sub.16 ]zH.sub.2 O, and h, k, n, s and t are number of cations or molecules and x, y, z and l are the same as mentioned in the foregoing.

However, the value of h varies with the s/t ratio as shown in the following table.

______________________________________Concentration in Concentration insubstrate solution zeolite OTWs/s+t h/x______________________________________100 % 100 % 16.67 % 99 % 9.07 % 98 % 1.98 % 67 % 0.99 % 45 %______________________________________

The zeolite OTW employed in this invention can be synthesized as follows:

The sources of Al, Fe, P and/or As are dissolved in water within the ranges (expressed in terms of molar ratios of their oxides) of 3.5 .ltoreq. (Al, Fe).sub.2 O.sub.3 /(P, As).sub.2 O.sub.5 .ltoreq. 4.5 and (K, Na).sub.2 O/(Al, Fe).sub.2 O.sub.3 >0.12.

As for the sources of Al and Fe to be employed according to this invention, there may be employed the metals as such, their chlorides, sulfides, nitrates, phosphates, arsenates and sulfates, such organic acid salts thereof as iron acetate, aluminum acetate, etc., alum containing either iron or aluminum, or their oxides and hydroxides and gels soluble in alkalis or acids. As the sources of P, use can be made of phosphorus pentoxide, phosphoric acid, and condensed acids which give phosphoric acid when dissolved in water, sodium phosphate, potassium phosphate, ammonium phosphate, (those phosphates include mono- and di-hydrogen salts), water-soluble calcium phosphate, strontium phosphate, and the like. As the souces of As, use can be made of arsenic pentoxide, arsenic acid, arsenous acid, sodium arsenate, potassium arsenate, ammonium arsenate (those arsenates include mono- and dihydrogen salts), and the like.

When these sources are not supplied with a sufficient amount of K or Na a hydroxide, an oxide or a salt of these metals must be added so as to satisfy the above ratio.

If the pH value of the resulting aqueous solution lies outside the range of 1 to 4, it is so adjusted by adding an alkali, an acid or a salt. FIGS. 1, 2, 3 and 4 respectively show pH ranges suitable for the attainment of zeolite OTW having the general formula (I) wherein l = 1, l = 0, y = 1 and y = 0.

Referring to these figures, the shaded area represents the pH range for crystals containing not only zeolite OTW, but also other compounds, while the cross-hatched area represents the pH range that will give zeolite OTW alone.

The pH-adjusted solution is heated at 100.degree. to 350.degree.C, desirably 150.degree. to 250.degree.C, until crystals separate, usually for 0.5 to a few hours. The heating is desirably carried out in a closed vessel or under conditions which will otherwise keep the solvent from being lost from the reaction system.

Then, the thus produced crystals are separated from the mother liquor by filtration.

The zeolite OTW employed in this invention essentially assumes a three-dimensional lattice structure which consists of an 8-membered oxygen ring of Al or Fe and a tetrahedron of phosphoric acid or arsenic acid. The ratio of elemental oxygen to the sum of (Al, Fe) and (P, As) is O/[(Fe,Al) + (P, As)]=16/7, at the time of synthesis, suitable numbers of univalent cations, e.g. potassium or sodium ion, as well as protons, are located in the crystal lattice for the balance of the valencies.

A characteristic X-ray powder diffraction pattern is available for zeolite OTW and can be utilized in the identification thereof. The x-ray powder diffraction pattern is set forth in Table 1.

Table 1______________________________________hkl d*1 (A) Intensity*2______________________________________100 8.02-7.47 FF110 5.67-5.28 ff111 4.63-4.31 F200 4.01-3.73 F210 3.59-3.34 f211 3.27-3.05 F220 2.84-2.64 F300 2.68-2.49 mF310 2.54-2.36 mF311 2.42-2.25 mF222 2.32-2.15 mF320 2.225-2.072 ff321 2.145-1.997 ff400 2.005-1.868 f410 1.945-1.813 f411 330 1.891-1.761 ff331 1.841-1.714 f420 1.794-1.671 f421 1.750-1.631 ff332 1.711-1.593 ff422 1.638-1.526 f500 430 1.604-1.494 f510 431 1.573-1.465 ff333 511 1.544-1.438 ff______________________________________ *1: d represents internal lattice spacing. *2: classification FF: very strong F: strong mF: rather strong f: weak ff: very weak?

EXAMPLE 1

In 1.5 liter of water is dissolved 600 g. of ammonium iron alum, and the solution is heated on a hot water bath. On the other hand, 160 g. of KH.sub.2 AsO.sub.4 and 150 g. of K.sub.2 CO.sub.3 are dissolved in water under heating on a hot water-bath to prepare 0.5 liter of a solution. Both solutions are mixed together gradually in such a manner that the pH of the resulting suspension becomes about 1.5. The mixed solution is put in a reactor, and heated at 220.degree.C for about 1 hour, so that crystals separate. The crystals are recovered by filtration and washed with a dilute acid. The crystals are further washed with distilled water until no sulfate ion is detected. The crystals are dried at 100.degree.C. The product zeolite OTW is of the formula KH.sub.4 Fe.sub.4 As.sub.3 O.sub.16.8H.sub.2 O.

Analysis: 0.47 K.sub.2 O, 2.00 Fe.sub.2 O.sub.3, 1.51 As.sub.2 O.sub.5, 8H.sub.2 O

The zeolite OTW has cubic unit cells characterized by the x-ray powder diffraction pattern shown in Table 2, wherein I and d denote relative intensities and internal lattice spacings, respectively, the unit cell constant a.sub.o thereof being 8.0A.

Table 2______________________________________hkl I d______________________________________100 100 8.01111 30 4.62200 30 4.00211 41 3.27220 40 2.83300 12 2.67310 22 2.53311 23 2.42222 6 2.313321 2 2.14400 4 2.003410 322 6 1.944411 8 1.887331 5 1.838420 14 1.792421 4 1.749422 8 1.634500 430 7 1.602______________________________________

0.018 Mole of the zeolite OTW is added to 200 ml. of a solution containing 0.1N of Ag.sup.+ and the mixture is heated on a hot water bath. The pH of the solution at this stage is about 4.0. After 15 minutes, the Ag.sup.+ -exchanged zeolite OTW is recovered by suction filtration and added to about 100 ml. of a previously heated 2N-nitric acid. The mixture is heated on a hot water bath for about 10 minutes, then the Zeolite OTW is filtered off. The residual solution is found to contain 3.15 grams as AgNO.sub.3 (93%).

EXAMPLE 2

0.01 Mole of Zeolite OTW (K.sub.1.4 H.sub.3.6 Fe.sub.4 As.sub.3 O.sub.16.7H.sub.2 O) is added to 200 ml. of pre-heated, solution containing 0.1N of Ag.sup.+ and the mixture as heated for about 15 minutes to cause an ion-exchange reaction. The pH of the solution at this stage is about 4.0. Then, the zeolite OTW is recovered by suction filtration with a glass filter, and washed with 50 ml. portion of a 2N-nitric acid, whereby 80 percent of the Ag.sup.+ contained in the zeolite OTW is recovered as a solution of AgNO.sub.3. Successive washing with further three 50 ml. portions of nitric acid increases the yield to 90%, 93% and 96%. The total amount of Ag.sup.+ thus recovered by the use of 0.01 mole of the zeolite OTW is 2.03 grams as AgNO.sub.3.

EXAMPLE 3

0.01 Mole of a zeolite OTW (K.sub.1.4 H.sub.3.6 Fe.sub.4 As.sub.3 O.sub.16.8H.sub.2 O) is added to 400 ml. of a solution containing 0.05N of Ag.sup.+ and 2.5N of Na.sup.+, and the mixture is heated on a hot water bath for about 20 minutes, to cause an ion-exchange reaction. The pH value of the suspension of the zeolite OTW at this stage is about 4.1. Then the ion-exchanged zeolite OTW is recovered by suction filtration and washed with four 50 ml. portions of a hot 2N-nitric acid. Ag.sup.+ contained in the respective washings is totaled to 1.35 grams as AgNO.sub.3, and the Ag.sup.+/Na.sup.+ ratio is 1.97. In other words, the concentration of Ag.sup.+ relative to Na.sup.+ in the original solution is heightened up to about 100 times. On the other hand, zeolite OTW recovered as above is washed with 50 ml. of a hot 2N-nitric acid. The washing is diluted with water to 4 times as much as its original volume, and then 0.007 mole of zeolite OTW is added as an ion-exchanger. When this solution is washed again with 50 ml. of a 2N-nitric acid, a nitric acid solution containing substantially Ag.sup.+ alone is obtained.

EXAMPLE 4

Sodium monohydrogen arsenate (312 g.) is dissolved in water and the resulting solution is gradually mixed with a solution of 648 g. of aluminum sulfate in 2 liters of water followed by the addition of an aqueous solution of sodium hydroxide, in such a manner that the pH of the entire mixture is adjusted to 4-5 and the total volume of the mixture is 4 liters. The mixed solution is heated at 225.degree.C for 90 minute, so that crystals are formed. The crystals are separated by suction filtration and washed with distilled water until no sulfate ion is detected. So washed crystals are dried at 100.degree.C. This product zeolite OTW is of the formula NaH.sub.4 Al.sub.4 As.sub.3 O.sub.16.8H.sub.2 O, the unit cell constant a.sub.o thereof being 7.69A.

Analysis: 0.53 Na.sub.2 O, 2.00 Al.sub.2 O.sub.3, 1.50 As.sub.2 O.sub.5, 8H.sub.2 O

0.01 Mole of the zeolite OTW is added to 400 ml. of a solution containing 0.05N of Ag.sup.+ and about 0.5N of Na.sup.+, and the mixture is heated on a hot water bath for about 15 minutes to cause an ion-exchange reaction. The pH value of the zeolite OTW containing solution at this stage is about 4.0. Then the ion-exchanged zeolite OTW is recovered by suction filtration with a glass filter and washed in the same manner as in Example 2. Ag.sup.+ contained in the washings is totaled to 2.01 g. as AgNO.sub.3. No Na.sup.+ is detected in the washing.

EXAMPLE 5

A solution of 500 g. of potassium-aluminum alum in 1 liter of water is poured gradually while stirring, in a solution of 200 g. of potassium monohydrogen phosphate in 1 liter of water. The pH of the mixed solution is adjusted to 9-9.5 with a potassium hydroxide solution. The mixed solution is put in a reactor. The reactor is sealed and maintained at 200.degree.C for 90 minutes, so that crystals are formed. The crystals are separated from the mother liquor by suction filtration and washed with distilled water until no more sulfate ion is detected in the washing. The crystals are then dried at 100.degree.C.

This product gives the following analysis:

0.51 K.sub.2 O, 2.00 Al.sub.2 O.sub.3, 1.50 P.sub.2 O.sub.5, 6.05 H.sub.2 O unit cell constant a.sub.o =7.474A.

The X-ray powder diffraction pattern of this product is shown in Table 3.

Table 3______________________________________hkl I d(A)______________________________________100 100 7.47111 15 4.32200 45 3.74211 50 3.05220 34 2.643300 20 2.490310 25 2.362311 7 2.255222 15 2.159321 5 1.999400 5 1.869410 10 1.813330 411 10 1.762331 3 1.715420 10 1.672332 4 1.595422 8 1.526500 7 1.495333 511 3 1.437______________________________________

0.02 Mole of thus produced zeolite OTW is treated after the manner in Example 1 to recover Ag.sup.+ in an amount of 3.23 g. as AgNO.sub.3 (95%).

EXAMPLE 6

A solution of 50 g. of sodium monohydrogen arsenate heptahydrate and 10 g. of potassium monohydrogen phosphate in 500 ml. of water is gradually added under stirring, 200 ml. of an aqueous solution of 95 g. of potassium-aluminum-alum. When the pH of the mixed solution becomes about 3.2 with the addition of an aqueous solution of potassium hydroxide on a hot water bath, the solution is put in a reactor. Then, the reactor is sealed and maintained at 200.degree.C for 3 hours, so that crystals are formed. The crystals are separated from the mother liquor by suction filtration and thoroughly washed with distilled water. The crystals are then dried at 100.degree.C.

This product gives the following analysis.

0.52 K.sub.2 O, 2.00 Al.sub.2 O.sub.3, 1.14 As.sub.2 O.sub.5, 0.38 P.sub.2 O.sub.5, 8H.sub.2 O unit cell constant a.sub.o =7.647A.

0.017 mole of thus produced zeolite OTW is treated after the manner in Example 1 to recover Ag.sup.+ in an amount of 3.11 g. as AgNO.sub.3 (91.5%).

EXAMPLE 7

Ammonium iron-alum (50 g.) and 47 g. of aluminum-alum are dissolved in water. To the resulting solution is gradually added an aqueous solution containing 35 g. of sodium arsenate and 7 g. of potassium phosphate so that the total volume of the mixture becomes 1 liter. The pH of the solution is adjusted to about 8-8.5 with potassium carbonate powder. While preventing a liquid loss, the solution is heated at 250.degree.C for about an hour, so that crystals are formed. The crystals are separated from the mother liquor by filtration and washed with distilled water until no more sulfate ion is detected in the washing. The crystals are then dried at 100.degree.C. This product gives the following analysis:

0.49 K.sub.2 O, 1.10 Fe.sub.2 O.sub.3, 0.98 Al.sub.2 O.sub.3, 1.15 As.sub.2 O.sub.5, 0.36 P.sub.2 O.sub.5, 7H.sub.2 O.

the unit cell constant a.sub.o is 7.79 A.

0.02 Mole of thus produced zeolite OTW is treated after the manner in Example 2 to recover Ag.sup.+ in an amount of 4.05 g. as AgNO.sub.3.

Claims

1. A method for the production of a zeolitic material represented by the formula:

R.sub.x H.sub.5.sub.-x (Al.sub.y Fe.sub.1.sub.-y).sub.4 (P.sub.l As.sub.1.sub.-l).sub.3 O.sub.16.zH.sub.2 O

wherein R represents Na or K, x, y, z and l are numerical values of 0.ltoreq.x.ltoreq.5, 0.ltoreq.y.ltoreq.1, z.ltoreq.9 and 0.ltoreq.l.ltoreq.1, respectively; which comprises preparing an aqueous solution by dissolving in water (1) at least one source of aluminum and iron selected from the group consisting of their chlorides, sulfides, nitrates, phosphates, arsenates, sulfates, acetates, oxides, hydroxides, gels soluble in alkalis or acids and alum containing either iron or aluminum, (2) at least one source of phosphorus and arsenic selected from the group consisting of phosphorus pentoxide, phosphoric acid, and condensed acids which give phosphoric acid when dissolved in water, sodium phosphate, potassium phosphate, ammonium phosphate, said phosphates including the mono- and di-hydrogen salts thereof, water-soluble calcium phosphate, strontium phosphate, aluminum phosphate, iron phosphate, arsenic pentoxide, arsenic acid, arsenous acid, sodium arsenate, potassium arsenate, ammonium arsenate, said arsenates including the mono- and di-hydrogen salts thereof, and (3) at least one source of sodium and potassium selected from the group consisting of their hydroxides, oxides and salts in the ranges expressed in terms of the molar ratios of their oxides of

3.5.ltoreq.(Al, Fe).sub.2 O.sub.3 /(P, As).sub.2 O.sub.5 .ltoreq.4.5 and (K, Na).sub.2 O/(Al, Fe).sub.2 O.sub.3 >0.12

adjusting the pH of the solution to within the range of the cross-hatched area in FIGS. 1 to 4 and heating the solution at 150.degree. to 250.degree.C in a closed vessel to crystallize the zeolitic material and recovering the objective zeolitic material.

2. A method as claimed in claim 1, wherein x, y, and l have numerical values of 0<x<5, 0<y.ltoreq.1 and 0<l.ltoreq.1, respectively, and the aqueous solution is prepared by dissolving (1) at least one source of aluminum or a mixture of at least one source of aluminum and at least one source of iron, (2) at least one source of phosphorus or a mixture of at least one source of phosphorus and at least one source of arsenic and (3) at least one source of sodium and potassium in water wherein the sources of components (1), (2) and (3) are as defined in claim 1.

3. A method as claimed in claim 1, wherein y and l have numerical values of 0<y<1 and 0<l<1, respectively, and the aqueous solution is prepared by dissolving (1) at least one source of aluminum, (2) at least one source of iron, (3) at least one source of phosphorus, (4) at least one source of arsenic and (5) at least one source of sodium and potassium in water wherein the sources of components (1) to (5) are as defined in claim 1.

4. A method as claimed in claim 1, wherein y and l have numerical values of 1 and 1, respectively, and the aqueous solution is prepared by dissolving (1) at least one source of aluminum, (2) at least one source of phosphorus and (3) at least one source of sodium and potassium in water in the ranges expressed in terms of the molar ratios of their oxides of

3.5.ltoreq.Al.sub.2 O.sub.3 /P.sub.2 O.sub.5 .ltoreq.4.5 and (K, Na).sub.2 O/Al.sub.2 O.sub.3 >0.12

and the pH of the solution is adjusted to within the range of the cross-hatched area in FIGS. 1 and 3 and wherein the sources of components (1) to (3) are as defined in claim 1.

5. A method as claimed in claim 1, wherein y and l are numerical numbers of 0<y<1 and 1, respectively, and the aqueous solution is prepared by dissolving (1) at least one source of aluminum, (2) at least one source of iron, (3) at least one source of phosphorus and (4) at least one source of sodium and potassium in water in the ranges of

3.5.ltoreq.(Al, Fe).sub.2 O.sub.3 /P.sub.2 O.sub.5 .ltoreq.4.5 and (K, Na).sub.2 O/(Al, Fe).sub.2 O.sub.3 >0.12

and the pH of the solution is adjusted to within the range of the cross-hatched area in FIG. 1 and wherein the sources of components (1) to (4) are as defined in claim 1.

6. A method as claimed in claim 1, wherein y and l are numerical values of 1 and 0<l<1, respectively, and the aqueous solution is prepared by dissolving (1) at least one source of aluminum, (2) at least one source of phosphorus, (3) at least one source of arsenic and (4) at least one source of sodium and potassium in water in the ranges of

3.5.ltoreq.Al.sub.2 O.sub.3 /P, As).sub.2 O.sub.5 .ltoreq.4.5 and (K,Na).sub.2 O/Al.sub.2 O.sub.3 >0.12

and the pH of the solution is adjusted to within the range of the cross-hatched area in FIG. 3 and wherein the sources of components (1) to (4) are as defined in claim 1.