Titanostannosilicates and preparation thereof

FIELD OF THE INVENTION
This invention relates to a new class of microporous materials composed of titanium, tin and silicon tetrahedral oxide units and having an unit empirical formula on a calcined and anhydrous basis of:
(Ti.sub.x Sn.sub.y Si.sub.z)O.sub.2
where "x" is the mole fraction of titanium and varies from about 0.005 to about 0.03, y is the mole fraction of tin and varies from about 0.0001 to about 0.01 and x+y+z=1. This invention also relates to a method of preparing these compositions.
BACKGROUND OF THE INVENTION
One of the most challenging and formidable tasks in preparative organic chemistry is the selective functionalization of hydrocarbons. Once a functional group has been introduced, the chemist has a rich selection of tools to achieve further transformations and transpositions, but the initial barrier of introducing a functional group is determinative of further chemistry. Not only is it necessary that a given functionalization reaction proceeds in good yield, but it is necessary also that it proceeds with specificity. One of the most chemically attractive entry points to functionalization of hydrocarbons is the carbon-carbon double bond in alkenes and substituted alkenes, for the carbon-carbon double bond undergoes many reactions which introduce functional groups onto one or both of the carbons, and the double bond also activates an adjacent C--H bond (i.e., allylic hydrogen) to still other reactions. Among the chemical reactions of the carbon-carbon double bond that of epoxidation occupies a special niche, because epoxidation is virtually unique to the C.dbd.C linkage, because epoxidation proceeds with great specificity, and because the resulting epoxide is a functional group which controllably reacts with a wide range of reagents, schematically represented here as H--Y, to afford an equally wide range of difunctional materials according to the reaction, ##STR1##
Although epoxidation may be performed with several different oxidizing agents, that variation of greatest interest here is one where the agent is a hydroperoxide. A commercial process uses tertiary butyl or ethylbenzene hydroperoxide in combination with 2% titania supported on silica to epoxidize propylene to propylene oxide with greater than 97% conversion of, for example, ethylbenzene hydroperoxide and selectivities to propylene oxide formation approaching 90%. See U.S. Pat. Nos. 3,642,833, 3,923,843, 4,021,454 and 4,367,342, all assigned to Shell Oil Company. More recently an Italian group has developed catalysts, referred to as titanium silicalites, where small amounts of framework silicon in silicalite are said to be replaced by titanium (Taramasso et al., U.S. Pat. No. 4,410,501), and has found such materials, conveniently designated as TS-1, to be effective in catalyzing the epoxidation of olefinic compounds by hydrogen peroxide in either the presence or absence of a solvent; U.S. Pat. No. 4,833,260. Subsequently this has been extended to the epoxidation of olefins with oxygen in air in the presence of a redox system of alkyl anthrahydroquinone and alkyl anthraquinone; EP 526,945.
Notari, B., Innovation in Zeolite Materials Science; Grobet, P. J. et al., Ed.,; Elsevier: Amsterdam, pp. 422-424 has speculated that the observed catalytic activity both of titania supported on silica and TS-1 arises from the high dispersion of titanium atoms in a silica lattice, that is, active materials are characterized by Ti(IV) isolated by a long sequence of --O--Si--O--Si--. This conclusion was supported somewhat by the observation that when titania is supported on alumina, magnesia, or zirconia the resulting composite is inactive in epoxidation, and also is supported by the observation that catalyst activity increases as manifested by an increase in epoxide selectivity as the concentration of titania on silica decreases. Catalytic activity of TS-1 in the hydroxylation of phenol with H.sub.2 O.sub.2 also has been shown to be dependent on particle size (A. J. H. P. van der Pol et al., Appl. Catal., A92 (1992), 113-130) with particles in the 0.2-0.3 micron range being 10 times more active than those in the 5 micron range.
More recently Nemeth et al. have shown that particular mixtures of a titanosilicate and titania are demonstrably more active and more selective as a catalyst in the epoxidation of olefinic compounds than are prior art titanium-based catalysts which have been used in epoxidation and have linked the improved catalytic qualities to the particle size of both the titanosilicate and titania; U.S. Pat. No. 5,466,835.
Applicants have synthesized a new family of titanostannosilicate molecular sieves which are microporous materials having a three-dimensional framework of titanium, tin and silicon tetrahedral units. These new compositions have been found to have improved epoxidation activity and durability. Applicants have also developed synthesis methods which can control the particle size and crystallinity of the molecular sieve. It has also been found that crystallinity and particle size affect the epoxidation activity of the molecular sieve.
SUMMARY OF THE INVENTION
The present invention relates to a family of titanostannosilicate molecular sieves and a process for preparing the molecular sieves. One embodiment of the invention is a crystalline titanostannosilicalite molecular sieve having a microporous framework structure of TiO.sub.2, SnO.sub.2 and SiO.sub.2 tetrahedral units and an unit empirical formula on an anhydrous and calcined basis of:
(Ti.sub.x Sn.sub.y Si.sub.z)O.sub.2
where "x" is the mole fraction of titanium and has a value of about 0.0005 to about 0.03, "y" is the mole fraction of tin and has a value of about 0.0001 to about 0.01 and "z" is the mole fraction of silicon and is defined by x+y+z=1.
Another embodiment of the invention is a process for preparing the titanostannosilicate described above. This process comprises forming a reaction mixture containing reactive sources of titanium, tin, silicon and a templating agent, A, at a temperature and a time sufficient to form the molecular sieve, the mixture having a composition expressed in terms of mole ratios of oxides of:
aA.sub.2 O:100SiO.sub.2 :bTiO.sub.2 :cSnO.sub.2 :dH.sub.2 O:eROH
where "a" ranges from about 12 to about 26, "b" ranges from about 1 to about 6.0, "c" --ranges from about 0.01 to about 1.0, "d" ranges from about 1200 to about 4000 and "e" ranges from 0 to about 250.
These and other objects and embodiments will become more apparent from the following detailed description of the invention.
DETAILED DESCRIPTION OF THE INVENTION
As stated, this invention relates to a new family of titanostannosilicate molecular sieves and to a process for preparing these molecular sieves. These molecular sieves are good catalysts for the epoxidation of olefins using peroxides as the oxidizing agent.
The titanostannosilicate compositions of this invention are crystalline microporous materials, i.e., molecular sieves, which have a three-dimensional framework structure of TiO.sub.2, SnO.sub.2 and SiO.sub.2 tetrahedral oxides. As is characteristic of molecular sieves, the present titanostannosilicate molecular sieves have uniform intracrystalline pores. These molecular sieves can be represented by a unit empirical formula on an anhydrous and calcined basis of:
(Ti.sub.x Sn.sub.y Si.sub.z)O.sub.2
where "x" is the mole fraction of titanium and varies from about 0.0005 to about 0.03, "y" is the mole fraction of tin and varies from about 0.0001 to about 0.03 and "z" is the mole fraction of silicon and is defined by x+y+z=1.
The molecular sieves of this invention can have various structures as defined by their x-ray diffraction pattern. One structure is that identified as silicalite which is an isotypic structure of MFI as defined in the "Atlas of Zeolite Structure Types" Meier et al., editors, Elsevier Publisher, Fourth Revised Edition, 1996, pp. 146-147.
Synthesis of the titanostannosilicates of this invention is carried out by a -hydrothermal crystallization of a reaction mixture prepared by combining reactive sources of titanium, tin, silicon, a templating agent, water and optionally an alcohol. Illustrative of the titanium sources which can be used in this invention include but are not limited to titanium alkoxides and titanium halides. Specific examples of titanium alkoxides are titanium tetraisopropoxide, titanium tetraethoxide and titanium tetrabutoxide, while specific examples of titanium halides are titanium trichloride and titanium tetrachloride. Preferred sources are titanium alkoxides and of these, titanium tetraisopropoxide is especially preferred. Illustrative of the silicon sources which can be used include but are not limited to colloidal silica, fumed silica and silicon alkoxides. Preferred sources are silicon alkoxides, examples of which are tetraethylorthosilicate and tetramethylorthosilicate. A preferred alkoxide is tetraethylorthosilicate. Finally, sources of tin include but are not limited to tin alkoxides and tin tetrachloride. Tin alkoxides include tin tetra t-butoxide. Tin tetrachloride is a preferred tin source.
The primary templating agent is tetrapropylammonium cation. This templating agent can be added as the hydroxide or as a salt such as the halide, nitrate, acetate, etc. It is preferred to add the templating agent as the hydroxide.
Generally, the hydrothermal process used to prepare the titanostannosilicate molecular sieve of this invention involves forming a reaction mixture which in terms of molar ratios of the oxides is expressed by the formula:
aA.sub.2 O:100SiO.sub.2 :bTiO.sub.2 :cSnO.sub.2 :dH.sub.2 O:eROH
where A is a templating agent, "a" ranges from about 12 to about 26, "b" ranges from about 1 to about 6.0, "c" ranges from about 0.01 to about 1.0, "d" ranges from about 1200 to about 4000 and "e" ranges from 0 to about 250. As the formula indicates, the reaction mixture can optionally contain an alcohol. It has been found that the addition of an alcohol produces a composition with smaller crystallite size (diameters) which in turn yields an improved epoxidation catalyst. Alcohols which can be used include isopropyl, ethyl and methyl alcohol with isopropyl alcohol being preferred.
The reaction mixture is prepared by mixing the desired sources of titanium, tin and silicon to give the desired mixture. It is also necessary that the mixture have a pH of about 9 to about 13. The basicity of the mixture is controlled by the amount of templating agent (if it is in the hydroxide form) which is added and the use of other basic compounds. The addition of other basic compounds may be needed if the templating agent is added as a salt, e.g., halide or nitrate. Examples of these basic compounds include ammonium hydroxide, quaternary ammonium hydroxides and amines. Specific examples include tetraethylammonium hydroxide, tetrabutylammonium hydroxide and tripropylamine.
Having formed the reaction mixture, it is next reacted at a temperature of about 100.degree. C. to about 175.degree. C. for a period of about 48 hours to about 96 hours in a sealed vessel under autogenous pressure. A preferred reaction temperature range is from about 125.degree. C. to about 150.degree. C. After the desired reaction time, the mixture is filtered to isolate the solid product which is washed with deionized water and dried in air.
As has been stated, the use of a mixed solvent, i.e., water/alcohol results in the production of molecular sieves with smaller crystallites. Thus, when water was the only solvent and colloidal silica was the silicon source, one obtained a product with average crystallite sizes of about 3 to about 10 micrometers, whereas when the solvent was an aqueous/alcoholic mixture and the silica source was tetraethylorthosilicate, particles of about 0.1 to about 10 micrometers were obtained.
As synthesized, the molecular sieves of this invention will contain some of the templating agent or the additional basic compounds in the pores. Upon calcination these cations are decomposed, yielding a protonic form of the sieve. These protons can be exchanged for other (secondary) cations. Generally, the exchangeable protons can be exchanged for alkali metal cations, e.g., K.sup.+, Na.sup.+, Rb.sup.+, Cs.sup.+, alkaline earth cations, e.g., Mg.sup.2+, Ca.sup.2+, Sr.sup.2+, Ba.sup.2+, or mixtures thereof. The methods used to exchange one cation for another are well known in the art and involve contacting the molecular sieve with a solution containing the desired cation at exchange conditions. Exchange conditions include a temperature of about 25.degree. C. to about 100.degree. C. and a time of about 20 minutes to about 24 hours. Finally, it should be pointed out that the as-synthesized molecular sieves can be calcined at a temperature of about 500.degree. C. to about 550.degree. C. which removes at least a portion of the templating agent.
As has been stated the molecular sieves of this invention are particularly suited as catalyst for the oxidation of olefinic compounds. The feedstock for the subject oxidation reaction contains olefinic compounds generally. The olefinic compound can be generally described according to the formula ##STR2## where R.sub.1, R.sub.2, R.sub.3, and R.sub.4 may be hydrogen, alkyl, aryl, cycloalkyl, aralkyl, carboxylic acid, carboalkoxy, a halogen, sulfonic acid, sulfonic acid ester, nitrile, sulfone, or ether group. The alkyl, cycloalkyl, arylalkyl, or aryl groups also may contain, e.g., a carboxylic acid grouping, carboxylic ester grouping, halogen, sulfonic acid or sulfonic ester grouping, nitrile, nitro, hydroxyl, ketone, anhydride, amino, hydroxyl, and ether groupings. As can be appreciated, our invention is applicable to an enormous diversity of olefinic compounds. In fact, the major criterion for a suitable feedstock is that it contain a non-aromatic carbon-carbon double bond.
One large group of olefinic compounds which may be used in the practice of our invention consists of the alkenes, especially those containing between about 2 and 20 carbon atoms. Such alkenes include ethylene, propylene, butene-1, butene-2, isobutylene, the pentenes, heptenes, hexenes, octenes, nonenes, decenes, undecenes, dodecenes, tridecenes, tetradecenes, pentadecenes, hexadecenes, heptadecenes, octadecenes, nonadecenes, and eicosene. Propylene, the butenes, pentenes, and hexenes (especially hexene-1) are particularly preferred in the practice of this invention. Dimers and trimers--and low-molecular weight oligomers generally--of the lower alkenes such as ethylene, propylene, and the butenes also are suitable olefinic compounds in the practice of this branch of the invention.
The cycloalkenes and the substituted cycloalkenes comprise another class of olefinic compounds which may be used in the practice of our invention. Suitable alkenes include cyclopentene, cyclohexene, cyclooctene, cycloheptene, cyclononene, and cyclodecene. Among other illustrative cyclic olefinic compounds are cyclooctadiene, dicyclopentadiene, methylenecyclopropane, methylenecyclopentane, vinylcyclohexene, methylcyclopentene, ethylcyclopentene, propylcyclopentene, methylcyclohexene, methylcycloheptene, and so forth.
Aryl substituted alkenes also may be used generally and include materials such as styrene, 1-phenyl-1-propene, 1-phenyl-2-propene, 2-phenyl-1-propene, the phenyl butenes, phenyl pentenes, phenyl hexenes, phenyl heptenes, divinylbenzene, indene, stilbene, and so forth.
The olefinic compounds which may be used in the practice of our invention may bear other functional groups, either at the olefinic carbons or, more generally, at a position other than the olefinic carbon. For example, alcohols and ethers thereof may be among the functionalized olefinic compounds used as a feedstock in our invention, including such materials as allyl alcohol, allyl methyl ether, allyl ethyl ether, 2-buten-1-ol, 3-buten-2-ol, 3-buten-1-ol, cinnamyl alcohol, alkyl and aryl ethers of the buten-1-ols, 2-methyl-2-propene-1-ol, alkyl ethers of the latter such as the methyl, ethyl, propyl, and butyl ethers, as well as such ethers as the benzyl and phenyl ethers thereof, all of which serve to illustrate the presence of an hydroxyl or ether group in the olefinic compound. Allyl alcohol and their ethers are particularly important inasmuch as the product, glycidol and glycidyl ethers, are important chemical intermediates.
Haloalkenes also may be used in the practice of this invention, particularly where the halogen is not on an olefinic carbon. For example, allyl chloride and allyl bromide afford as the epoxidation product epichlorohydrin and epibromohydrin, resp., both of which are important articles of commerce.
Olefinic carboxylic acids and their esters are another class of compounds which may be used in the practice of our invention and may be exemplified by such materials as acrylic acid, alpha-methacrylic acid, 2-butenoic acid, 3-butenoic acid, 2-pentenoic acid, 3-pentenoic acid, 4-pentenoic acid, 2-methyl-2-butenoic acid, 3-methyl-2-butenoic acid, 2-methyl-3-butenoic acid, and so forth. Other unsaturated acids of particular mention as olefinic compounds subject to epoxidation by the process of our invention include cinnamic acid, maleic acid, and fumaric acid, and the large class of unsaturated fatty acids and their esters, especially triglycerides, represented by acids such as linoleic acid, linolenic acid, oleic acid, ricinoleic acid, erucic acid, palmitoleic acid, and the like.
Other functional groups may be present in the olefinic compound, especially at the non-olefinic carbons, including such functional groups as the sulfonic acid grouping and their corresponding esters, the nitrile grouping, nitro and ether grouping. Dienes also may be used in epoxidation, especially butadiene. Except in unusual circumstances it must be recognized that dienes can be expected to undergo epoxidation at either C.dbd.C bond, hence the selectivity of the epoxidation of dienes can be expected to be low with respect to formation of an epoxide at but one point in the molecule. Consequently dienes, and polyenes more generally, are not favored among the olefinic compounds for this reaction, principally because of the complexity of the resulting reaction mixture. On the other hand, where selectivity of double bond epoxidation is unimportant polyenes may be readily numbered as among the suitable substrates in our invention.
The preferred epoxidizing agent of our invention is hydrogen peroxide, although organic hydroperoxides may be used but not necessarily with equivalent results. Among the organic hydroperoxides may be mentioned the alkyl hydroperoxides, especially tertiary butyl hydroperoxide and, to a lesser extent, the hydroperoxide of ethylbenzene. Peracids form another class of organic compounds furnishing the peroxide linkage and among these peracetic acid, trifluoroperacetic acid, and perbenzoic acid are the most commonly employed peracids.
The primary oxidizing agent which is used in the practice of this invention is hydrogen peroxide, especially as aqueous solutions. Thirty weight percent solutions of hydrogen peroxide in water have been standard in the prior art, but their disadvantage is that of cost. One important advantage of the process of our invention is that our catalysts are effective in bringing about epoxidation even with a feed containing dilute aqueous hydrogen peroxide as the oxidizing agent. Thus, feedstocks containing even 2 weight percent aqueous hydrogen peroxide solutions may be employed to convert the olefinic compounds present to their epoxide in yields in excess of 90% and with virtually 100% efficiency in utilization of hydrogen peroxide. In general, feedstocks containing as little as about 2% and as much as about 70 weight percent hydrogen peroxide may be used, although hydrogen peroxide concentrations of 2-15 weight percent are far more common, and concentrations of 2-10 weight percent are preferred. Where the olefinic compound is epoxidized under heterogeneous conditions, it behooves one to use as concentrated a hydrogen peroxide as is readily available, which generally translates to the use of a 30% hydrogen peroxide solution. Nonetheless, we need to emphasize again that the concentration of the hydrogen peroxide in the feedstock is not a controlling factor in the practice of our invention, that dilute hydrogen peroxide solutions can be readily employed, and that the concentration of hydrogen peroxide used is dictated by secondary factors extraneous to our invention itself.
Olefinic compounds are oxidized using principally hydrogen peroxide as the oxidizing agent in the presence of the aforedescribed catalyst under epoxidation reaction conditions. Such reaction conditions include a temperature as low as about 0.degree. C. up to as high as about 100.degree. C. However, where hydroxyl-containing solvents are present, as usually 10 is the case since aqueous hydrogen peroxide is the most common peroxide source, epoxides frequently react with the hydroxylic component at temperatures above about 50.degree. C. In such instances temperatures in the range 0-50.degree. C. are preferred, especially those in the 30-45.degree. C. interval. Epoxidation may be conducted at atmospheric pressure, although a major reason to perform the epoxidation at elevated pressure is to increase the solubility of gaseous reactants in the reaction medium. For example, where propylene is epoxidized without the use of a cosolvent increased pressure leads to an increased solubility of the propylene in aqueous solution with an increase in overall rate of propylene epoxide formation. In a greatly preferred variant epoxidation is performed in aqueous alcohols, especially alcohols having fewer than 5 carbons. We particularly prefer conducting epoxidations in aqueous methanol as the solvent system. Other water-miscible cosolvents also may be employed. For example, acetone and water-soluble ethers such as dioxane, tetrahydrofuran, and ethers of ethylene glycol and poly(ethylene glycol)--the glymes--may be fruitfully used. In another variant the feed contains from 2 up to 200 ppm of a buffer, preferably between about 5 and 20 ppm, with potassium acetate being especially useful.
Epoxidation may be performed according to our invention in either a batch or continuous mode. For example, in a batch mode the olefinic compound, either alone or in an organic solvent, is mixed with an aqueous hydrogen peroxide solution in the presence of an effective amount of our catalyst. The amount of titanostannosilicate used per mole of carbon-carbon double bond to be epoxidized may be as low as about 3 grams per mole. There is no theoretical limit to the maximum amount of titanostannosilicate to be used, although as a practical matter there is no benefit from using more than about 30 grams per mole of carbon-carbon double bond. The reaction mixture is stirred well at temperatures between 0.degree. C. up to as high as about 100.degree. C., although in hydroxylic solvents the practical upper limit is about 80.degree. C. The hydrogen peroxide may be present at a concentration as low as about 2 weight percent and as high as about 50 weight percent. Whether the hydrogen peroxide or the olefinic compound is present in excess depends upon the nature of the olefinic compound as well as its cost. For example, where propylene is being epoxidized, unreacted gaseous propylene may be readily recovered and recycled. In such an instance it is advantageous to have the olefinic compound in molar excess, perhaps as much as 2-5 moles per mole of hydrogen peroxide. However, where a rather expensive, or relatively unavailable, olefinic compound is being epoxidized, it may be highly advantageous to use hydrogen peroxide in molar excess, perhaps in amounts as little as 5-10% molar excess, although molar ratios of up to 5 may be employed. In general, then, the molar ratio of olefinic compound to hydrogen peroxide may range from 1:5 to 5:1.
Where the reaction is performed in a continuous mode one may employ any of the conventional process techniques currently known. These include use of a fixed bed process, a continuous stirrer tank reactor process, a radial bed reactor process, and so on. In such cases the catalyst of our invention may be used as pellets, extrudates, spheres, and the like. When our catalyst is used in such forms it is preferable to incorporate a binder for preserving and enhancing catalyst integrity. Conventional binders include silica, alumina, silica-alumina, and various clays, but since such conventional materials are well known to those skilled in the binder art no further detailed discussion will be given. The exothermicity of the epoxidation reaction and activity of our materials also requires dilution of the active molecular sieve component in the catalyst bed to a maximum of about 18 weight percent titanostannosilicate. At this dilution the heat of reaction is readily controlled.
It has been found that an average crystallite size (i.e. average crystallite diameter) of the titanostannosilicate molecular sieve no more than about 0.5 micrometers is greatly preferred and that sieves with an average crystallite size of no more than about 0.3 micrometers are still more highly preferred. When synthesis is performed in an aqueous/alcoholic medium the requisite small crystallite size sieve results upon hydrothermal crystallization without added or special procedures, which is one reason that this synthetic mode is favored.
In order to more fully illustrate the invention, the following examples are set forth. It is to be understood that the examples are only by way of illustration and are not intended as an undue limitation on the broad scope of the invention as set forth in the appended claims.

EXAMPLES
Preparation of a Titanostannosilicalite: 700 g TEOS (tetraethylorthosilicate) and 57.90 g Ti(O-iPr).sub.4 were placed in a large beaker and stirred vigorously. Separately, 468.8 g TPAOH (tetrapropylammonium hydroxide) (40%) was diluted with 600 g deionized water. This solution was added in a fast dropwise fashion to the stirring alkoxides. In the first few minutes of the additions a white precipitate begins to appear, but it redissolves as more TPAOH solution is added. At the end of the addition the mixture is a clear colorless solution. This is allowed to stir 30 minutes. A solution is prepared by dissolving 11.55 g SnCl.sub.4 .multidot.5H.sub.2 O in 68 g deionized water. This is then added dropwise to the reaction mixture. At the end of this addition, the reaction mixture is still a solution. The reaction mixture is then vigorously stirred for another hour before it is placed in an autoclave with stirring capabilities. The mixture is digested for 72 hours at 150.degree. C.
The products solids are isolated, washed with deionized water, and dried at 120.degree. C. The dried solid is then calcined at 550.degree. C. in air to form the catalyst. The infrared spectrum of calcined material shows a band at 962 cm-1, which is consistent with reports of framework titanium in the silicalite structure. The ultraviolet-visible spectrum shows absorbance at approximately 210 nm, which is associated with framework-incorporated titanium. Extra-framework titania, which is characterized by a broad absorbance from 285-350 nm, was absent as indicated by no significant absorbance within the aforementioned range.
X-Ray Diffraction Data. The X-ray diffraction data summarized in table 1 are typical of the titanostannosilicalites prepared and are indicative of the silicalite structure. The broad line widths are due to the small (ca. 0.1.mu.) crystallite size. The results presented are for calcined material, with appreciable variation often noted between calcined and uncalcined material. The d-spacings can vary +/-0.25 angstroms.
TABLE 1______________________________________X-Ray Diffraction Data for a Calcined Titanostannosilicalite2-theta(deg) d (angstroms) Intensity______________________________________ 8.02 11.01 vs 8.93 9.89 s13.31 6.64 w14.03 6.30 w14.92 5.93 m15.63 5.66 w16.02 5.53 w17.85 4.96 w19.39 4.57 w20.97 4.23 w23.27 3.82 s23.88 3.72 m24.08 3.69 m29.44 3.03 w30.12 2.96 w45.32 1.99 w24.56 3.62 w______________________________________
X-Ray Photoelectron Spectroscopic Analysis. As evidence of the framework incorporation of tin into the titanium silicalite structure, X-ray photoelectron spectroscopy was utilized to measure the Ti/Si and Sn/Si ratio at both the surface and in the bulk of sample crystals. Sample A was prepared by tin impregnation of a titanium silicalite. A 10 gram sample of TS-1 was impregnated with an aqueous solution of SnCl.sub.4. The sample was dried, then calcined at 550.degree. C. Sample B was prepared via a precursor gel formation from titanium, tin, and silicon sources. Results are tabulated below.
TABLE 2______________________________________X-ray Photoelectron Spectroscopic Analysis Ti/Si Sn/SiSample surface bulk surface bulk______________________________________A 0.016 0.019 0.0120 0.0021B 0.015 0.015 0.0030 0.0026______________________________________
These data clearly show that the Sn/Si ratio differs for surface and bulk measurements in sample A, but are identical at the surface and bulk in sample B. This is convincing evidence for the presence of tin in the framework of sample B.
X-Ray Absorbtion Near Edge Spectroscopy (XANES). This analytical technique was applied to determine the local bonding geometry and oxidation state of some titanostannosilicalites. The data were collected on beamline X19A at the National Synchrotron Light Source, Brookhaven National Laboratory. The x-rays were monochromatized with an NSLS boomerang-type flat crystal monochromator with Si(111) crystals and collimated with an Al-coated glass mirror (critical energy 11 keV). The harmonic content was reduced by detuning the monochromator crystals by 30%. The XANES spectra were measured as fluorescence yield excitation spectra using a Lytle-type detector with nitrogen gas. The incident beam intensity was monitored with a split ion chamber with a constant purge of He. The incident beam size was approx. 1 mm.times.1 mm. The XANES of the reference compounds were measured as either electron yield spectra (using a detector manufactured by The EXAFS Co.), or as fluorescence yield spectra of material diluted to approx. 1 wt. % in BN. To minimize absorption by the air, the detector was placed close to the end of the beam pipe. All of the spectra were collected at room temperature. The monochromator was calibrated using Ti (4966.0 eV), V (5465.0 eV) and Sn (3929.0 eV) reference foils.
Spectra were processed using the BAN software package. The energy scales were established by setting the maximum of the first derivative of the XANES spectrum of the metal foils to 0.0 eV. Thus for the Ti K-edge data, 0.0 eV=4966.0 eV. The background was approximated by a least squares fit of the pre-edge region (-45 to -10 eV) and was subtracted from the spectrum. The spectra were then normalized to unity absorption by using a single point normalization well above the absorption edge. This normalization process is expected to give spectra that can be qualitatively compared only.
The Ti K-edge XANES of three Ti reference compounds were studied: anatase, TiO.sub.2 ; barium orthotitanate, Ba.sub.2 TiO.sub.4 ; and fresnoite, Ba.sub.2 TiSi.sub.2 O.sub.8. The spectra of all three compounds have one or more prominant pre-edge absorption features before the main absorption edge itself. The spectra of barium orthotitanate and fresnoite have a single feature, whereas anatase shows a triplet. These features have been well-studied in the literature, and indeed accurate information on the local coordination environment of the Ti can be derived if both the pre-edge position and height are known (F. Farges, G. E. Brown, J. J. Rehr, Geochim. Et Cosmo. Acta, 60 (1996) 3023). These features are attributed to transitions from the is energy levels of Ti to the Ti 3d/O 2p molecular orbitals. A is to 3d transition is forbidden by dipole selection rules but becomes allowed when p-d orbital mixing occurs in a site without a center of symmetry e.g. when Ti is located in a TiO.sub.4 tetrahedron. The height and position of the pre-edge feature are direct functions of the degree of p-d mixing and oxidation state. From the large body of data that has been acquired on Ti--O reference materials three main domains of height/position can be identified for 4-, 5- and 6-coordinated Ti (F. Farges et. al, op. cit.). The data summarized in Table 3 are in excellent agreement with the published values.
TABLE 3______________________________________Ti Reference Compounds Ti Pre-edge peak Pre-edgeCompound coordination position (eV) peak height______________________________________Ba.sub.2 TiO.sub.4 Barium 4 4969.0 0.65 orthotitanateBa.sub.2 TiSi.sub.2 O.sub.8 Fresnoite 5 4970.2 0.31TiO.sub.2 Anatase 6 4971.5 0.17______________________________________
The spectra of the titanostannosilicalite samples G and H are dramatically different. The spectrum from sample H shows a single intense pre-edge feature, whereas that from sample G shows a spectrum more similar to that of anatase. The position and height of the pre-edge peak from sample H indicates that the Ti is 4-fold coordinate. A spectrum fit to that of 77% anatase +23% sample H shows reasonable agreement to that of sample G. Thus, while all the Ti in sample H is 4-fold coordinate (and therefore all framework Ti), 77.+-.5% of the Ti in sample G is present as anatase-like titanium, and is thus extra-framework. Moreover, from the ratio of the step heights of the absorption edge itself, there is 4.4 times as much Ti in sample G than in sample H.
Oxidation with Titanosilicalites and Titanostannosilicalites. Catalytic Testing. Hydrogen peroxide (40 g, 30 weight percent concentration of H.sub.2 O.sub.2), 200 g methanol, and 5 g catalyst were loaded to 300 cc stainless steel autoclave. At room temperature was charged 80 g liquid propylene with nitrogen. The pressure was increased with nitrogen to 500 psi and the temperature was increased to 40/C over 30 min. The molar ratio of propylene to H.sub.2 O.sub.2 under these conditions is 5; H.sub.2 O.sub.2 is the limiting reagent. Liquid samples were taken at 1,3, 4 and 6 hrs. After 6 hrs the reaction was shut down and the autoclave was depressured. The remaining liquid was sampled again. This final sample is termed the "shut-down" sample.
The samples were analyzed by GC. The yield of propylene oxide is expressed as concentration of propylene oxide in the sample to the maximum theoretical concentration of propylene oxide. (Yield=[Propylene oxide]/[Propylene oxide].sub.max theoretical) The selectivity to propylene oxide is calculated as the ratio of the concentration of propylene oxide in the sample to the sum of the concentrations of propylene oxide, methoxy-propylene glycols, and propylene glycol. The batch autoclave results for the Ti--V silicalites prepared via aqueous and non-aqueous routes are shown below.
TABLE 4__________________________________________________________________________Propylene Oxidation with Various SilicalitesMolar Ratio in Gel Crystallization Atomic Ratio in SieveSample Si Ti Sn H.sub.2 O TPAOH Temp., .degree. C. Si/Ti Si/Sn Yield Selectivity__________________________________________________________________________A.sup.b 47 45 71B 100 3 0.3 3760 .sup. 33.sup.a 175 64 390 64 77C 100 3 0.3 3760 .sup. 33.sup.a 175 24 200 88 87D 100 3 1 3015 .sup. 33.sup.a 150 57 70 39 46E 100 6 1 1400 32 100 144 836 51 91F 100 6 1 3000 45 160 55 377 83 87G 100 6 1 1600 28 175 20 146 62 80H 100 6 1 1600 28 150 66 150 74 75I 100 6 1 1600 28 125 80 364 66 76J 100 6 1 1600 28 100 135 1125 49 84K 100 5 0 1616 28 100 143 0 30 88L 100 5 0 1616 28 125 63 0 47 89M 100 5 0 1616 28 150 51 0 56 85N 100 5 0 1616 28 175 21 0 45 56__________________________________________________________________________ .sup.a = 142 Parts isopropyl alcohol .sup.b = Sample of TS1 provided by PUNA National Laboratory, India.

Number	Name	Date
4329328	McAnespie et al.	May 1982
4410501	Taramasso et al.	Oct 1983
4833260	Neri et al.	May 1989
5110571	Corcoran et al.	May 1992
5155243	Fjuiwa et al.	Oct 1992
5208006	Kuznicki et al.	May 1993
5246688	Faust et al.	Sep 1993
5399336	Guth et al.	Mar 1995
5463090	Rodriguez et al.	Oct 1995
5466835	Nemeth et al.	Nov 1995
5646314	Crocco et al.	Jul 1997
5648558	Hatano et al.	Jul 1997

Titanostannosilicates and preparation thereof

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Fejes et al., "Synthesis of tin (IV) silicalites (MFI) and their characterization: A Mossbauer and MAS NMR spectroscopic study", Applied Catalysis A: General, 145 (1996) 155-184 (No Month).