Abstract: The present invention is directed to a process for the carbonylation of an arylene to an arylaldehyde (e.g., toluene to tolualdehyde) in the presence of a solid acid catalyst. The process for making tolualdehyde comprises carbonylating toluene in the presence of either carbon monoxide or a source of carbon monoxide and in contact with a solid acid catalyst. The reaction is carried out at a temperature ranging from -40.degree. to 200.degree. C., and at a pressure ranging from 20-4000 psig.

Abstract: Anions of the formula (I):[DA.sub.5 M.sub.30-x O.sub.110-x (M'L).sub.x ].sup.m- (I)in which D is Na.sup.+, Ca.sup.2+ ; A is P, As, Sb, Si, Ge, or combinations thereof, M is W.sup.5+, W.sup.6+, or mixtures thereof; M' is a metallic element from groups 2 to 15 of the periodic table; other than W; L is O.sup.2-, OH.sup.-, H.sub.2 O; x is 0-10; and m is 10-20; selectively react with cations Z.sup.n+ to afford anions of the formula (II):[ZA.sub.5 M.sub.30-x O.sub.110-x (M'L).sub.x ].sup.(m+1-n)-(II)wherein n is 3 or 4; Z=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Y, or Bi, when n=3, and Z=Ce, U, Np, Pu, or Am, when n =4. This reaction may be used for the selective encapsulation of lanthanide or actinide cations, and salts containing anions of formula (II) may be vitrified to form glasses or reduced to form tungsten "bronze" materials suitable for the long-term storage of radioactive lanthanides or actinides.

Abstract: A microporous crystalline silico-alumino-phosphate RUW-18, the theoretical composition of which, on a water-free basis after synthesis and calcination, is: H.sub.x Si.sub.x Al.sub.y P.sub.z O.sub.2 where x has a value between 0.005 and 0.1 and y and z are values between 0.4 and 0.6. The product has an AEI structure and possesses acidic properties. A procedure for manufacturing the product is also described. RUW-18 is suitable as a sorbent and as a catalyst in the manufacture of olefins from methanol.

Abstract: Glycol ether compounds such as glycol ethers and glycol ether esters are used as azeotropic distillation solvents for conversion of inorganic oxide hydrogels to xerogels by removal of water. These compounds are especially useful to make chromium-containing catalysts for production of high melt index polyolefins at reduced cost compared to known azeotropic solvents.

Abstract: Phosphomagnesia compositions settable into improvedly water-insensitive cements that retain their mechanical properties comprise an intimate admixture of (i) a binder phase including (a) at least one phosphorous compound (P.sub.2 O.sub.5 or derivative/precursor thereof) and (b) at least one magnesium compound reactive therewith in the presence of water, (ii) an effective amount of cementitious aggregate, and (iii) a water sensitivity-reducing amount of at least one silicone homogeneously distributed therethrough.

Abstract: Electroluminescent phosphors having substantially increased luminance and maintenance over that of prior art electroluminescent phosphors may be made by (1) doping an inorganic intercalation compound having an atomic structure interspersed with vacant spaces, with selected activator ions capable of luminescent emission, and (2) introducing organic monomers or other conductive material into the vacant spaces of the atomic structure of the doped inorganic intercalation compound. The organic monomers may be polymerized in situ to form conductive polymers therein.

Abstract: There is provided a method for making a divalent or polyvalent organic anion-intercalated hydrotalcite-like materials by first reacting a magnesium-containing powder and a transition alumina powder in an aqueous suspension to form a meixnerite intermediate. This intermediate is then contacted with a dicarboxylate or polycarboxylate anion to form a hydrotalcite-like material. The latter is then separated from the suspension. Representative materials include an oxalate-, succinate- or terephthalate-intercalated hydrotalcite-like material.

Abstract: Inorganic intercalation phosphors were made by doping an inorganic intercalation compound having an atomic structure interspersed with vacant spaces with selected activator ions capable of luminescent emission when excited by ultraviolet light and/or cathode rays.

Abstract: An electrorheological fluid that includes a dispersed particulate phase of anhydrous amorphous ceramic particles. The anhydrous amorphous ceramic particles can be of a very precisely tailored composition that is unavailable in crystalline form, for obtaining enhanced electrorheological response. The amorphous particles are substantially free of water when used, and have reduced tendency to absorb water in use. Accordingly, the electrorheological fluid containing anhydrous amorphous electrorheologically responsive ceramic particles has wide applicability for use, and enhanced durability in such use.

Abstract: A process for producing a precursor of a phosphorus-vanadium oxide catalyst for production of maleic anhydride by vapor phase oxidation of a hydrocarbon having 4 carbon atoms, which comprises reacting phosphoric acid and a pentavalent vanadium compound in an organic solvent capable of reducing at least a portion of the pentavalent vanadium to a valence state of +4, the phosphoric acid being substantially composed of orthophosphoric acid, and a phosphoric acid solution whose concentration is 88 to 96% being used as a source of the phosphoric acid; and a process for producing the catalyst comprising dry-pulverizing the catalyst precursor.

Abstract: Phosphomagnesia compositions settable into improvedly water-insensitive cements that retain their mechanical properties comprise an intimate admixture of (i) a binder phase including (a) at least one phosphorous compound (P.sub.2 O.sub.5 or derivative/precursor thereof) and (b) at least one magnesium compound reactive therewith in the presence of water, (ii) an effective amount of cementitious aggregate, and (iii) a water sensitivity-reducing amount of at least one silicone homogeneously distributed therethrough.

Abstract: Electroluminescent phosphors having substantially increased luminance and maintenance over that of prior art electroluminescent phosphors may be made by (1) doping an inorganic intercalation compound having an atomic structure interspersed with vacant spaces, with selected activator ions capable of luminescent emission, and (2) introducing organic monomers or other conductive material into the vacant spaces of the atomic structure of the doped inorganic intercalation compound. The organic monomers may be polymerized in situ to form conductive polymers therein.

Abstract: Three families of ceramic compositions having the given formula: .phi..sub.1+X Zr.sub.4 P.sub.6-2X Si.sub.2X O.sub.24, .phi..sub.1+X Zr.sub.4-2X Y.sub.2X P.sub.6 O.sub.24 and .phi..sub.1+X Zr.sub.4-X Y.sub.X P.sub.6-2X Si.sub.X O.sub.24 wherein .phi. is either Strontium or Barium and X has a value from about 0.2 to about 0.8 have been disclosed. Ceramics formed from these compositions exhibit very low, generally near neutral, thermal expansion over a wide range of elevated temperatures.

Abstract: This invention presents a novel MgAPSO molecular sieve, containing a critical range of magnesium: in the sieve framework and having a small crystallite size, which is particularly active for hydrocarbon conversion. The sieve advantageously is incorporated, along with a platinum-group metal, into a catalyst formulation which is useful for isomerization. When utilized in a process for isomerizing a non-equilibrium mixture of xylenes containing ethylbenzene, a greater yield of para-xylene is obtained compared to prior-art processes.

Abstract: This invention provides new inorganic composite materials for hard tissue replacement. The new composite material comprises solid material of calcium sulfate which is fully or partially converted to calcium phosphate from aqueous solution. This composite material has good biocompatibility and controllable resorption, and will be very useful for bone substitute material in orthopaedic and dental applications. The fully converted material which comprises mainly apatite calcium phosphate is also useful for chromatography application. A process to prepare these new composite materials is also described.

Abstract: A process for producing an antimicrobial compound represented by the following formula [1]:M.sup.1.sub.a H.sub.b A.sup.1.sub.c M.sup.2.sub.2 (PO.sub.4).sub.3.nH.sub.2 O [1]wherein M.sup.1 is at least one metal ion selected from silver, copper, zinc, tin, mercury, lead, iron, cobalt, nickel, manganese, arsenic, antimony, bismuth, barium, cadmium and chromium, A.sup.1 is at least one ion selected from alkali metal ion and alkaline earth metal ion, M.sup.2 is a tetravalent metal, n is a number which satisfies 0.ltoreq.n.ltoreq.6, a and b are positive numbers and c is 0 or a positive number, and a, b and c satisfy ka+b+mc=1 where k is a valence of M.sup.1 and m is a valence of A.sup.1, by supporting at least one metal ion selected from silver, copper, zinc, tin, mercury, lead, iron, cobalt, nickel, manganese, arsenic, antimony, bismuth, barium, cadmium and chromium on a phosphate represented by the following formula [2]:A.sup.2.sub.d M.sup.2.sub.2 (PO.sub.4).sub.3.nH.sub.2 O [2]wherein A.sup.

Abstract: Compounds that satisfy the general formula A.sub.1-Y.sup.4+ A.sub.Y.sup.1+ A.sub.Y.sup.3+ V.sub.2-X E.sub.X O.sub.7 exhibit isotropic NTE behavior above a temperature of about 100.degree. C. Y is from about 0.0 to about 0.4, and more preferably is about 0.2. X is from about 0.6 to about 1.4, and is more preferably about 1. Particularly suitable NTE compounds have X about 1 and Y about 0. A.sup.4+ is selected from the group consisting of Hf, Zr, Zr.sub.a M.sub.b, Hf.sub.a M.sub.b and mixtures thereof wherein a plus b equals one and M is selected from the group consisting of Ti, Ce, Th, U, Mo, W, Pb, Sn, Ge and Si. More preferably, A.sup.4+ is selected from the group consisting of Hf and Zr. A.sup.1+ is selected from the group consisting of the alkali earth metals, A.sup.3+ is selected from the group consisting of the rare earth metals, and E is selected from the group consisting of P and As. The NTE materials may be incorporated into compositions such as epoxy and ceramic compositions.

Abstract: Halogen-containing synthetic resins can be stabilized with calcium and/or zinc soaps. Co-stabilizers are necessary for enhancing their stabilizing effect. The invention relates to special cationic layered hydrotalcite compounds having a specific BET surface of at least 50 m.sup.2 /g which are modified with polyols, epoxidized esters, full and partial esters of polyols and/or phosphites, to a process for their production and to their use as co-stabilizers for halogen-containing synthetic resins stabilized with calcium and/or zinc salts.

Abstract: A process is disclosed for treating a crystal of MTiOXO.sub.4 which has crystal structure deficiencies of M and O, wherein M is selected from the group consisting of K, Rb, Tl and NH.sub.4 and mixtures thereof and X is selected from the group consisting of P, As and mixtures thereof, which includes the step of heating said crystal in the presence of a mixture of MTiOXO.sub.4 and at least one inorganic compound of one or more monovalent cations selected from the group consisting of Rb+, K+, Cs+ and Ti+ (said inorganic compound(s) being selected to provide a source of vapor phase monovalent cation and being present in an amount sufficient to provide at least a 0.1 mole % excess of the monovalent cation in relation to the M in the MTiOXO.sub.4 in said mixture) at a temperature of from about 400.degree. C. to 950.degree. C. and a pressure of at least 14 psi, and in the presence of a gaseous source of oxygen for a time sufficient to decrease the optical damage susceptibility of said crystal.

Abstract: A composition comprising a crystalline aluminumphosphate material having a three-dimensional microporous crystal framework structure whose chemical composition expressed in terms of mole ratios of oxides isAl.sub.2 O.sub.3 : 1.0.+-.0.2 P.sub.2 O.sub.5 ;and which is further defined as having an x-ray powder diffraction pattern characterized by d spacings at less than about 40 degrees two-theta as measured using copper K-alpha radiation that are substantially as shown in the Table and a metal in an amount of up to about 25 percent by weight is disclosed. The composition can be prepared by impregnating the crystalline aluminumphosphate material with the metal in an amount of up to about 25 percent by weight. The resultant heterocatalyst system can be used to shape-selectively hydrogenate an unsaturated organic compound, such as, for example an olefin, aldehyde or ketone.

Abstract: An improved method is disclosed for preparing zinc polyphosphate in a stable, concentrated solution, for water treatment purposes having a pH above 7.0 and in a preferred range of pH between 8.0 and 10.0. Without any acid solubilization required, an approximate 60% solution of tetrapotassium pyrophosphate (TKPP) is formulated and mixed thoroughly in a tank or similar container. Under constant stirring, a predetermined aqueous solution of a normal zinc salt, such as zinc chloride, gradually injected and mixed together into the TKPP solution at a preferred rate of about 5% of the zinc salt solution per minute and in a sufficient amount determined to add about 1 part of zinc to between 5-8 parts of TKPP by weight for maximum corrosion protection.

Abstract: A controlled slow release potassium divalent metal phosphate composition for agriculture and an effective method of preparing the composition. The cold water insolubilities of each of the contained nutrients are between 35 and 98 percent. The potassium exhibits an Activity Index between 20 and 85. The release of all contained nutrients is substantially complete in one growing season without damage to plant foliage or roots. Divalent metals effectively forming the new composition include magnesium, manganese, zinc, iron, cobalt, and copper. The effective method of preparing the new composition requires the exothermic coreaction of concentrated potassium hydroxide, divalent metal oxide powder, and concentrated phosphoric acid, with a molecular ratio of 1 potassium/1 divalent metal/1 phosphate with the total water content of the initial reaction mixture between 20 and 50 percent, at a maximum temperature between 85.degree. and 150.degree. C.

Abstract: Crystalline aluminumphosphate compositions having three-dimensional microporous crystal framework structures whose chemical composition expressed in terms of mole ratios is Al.sub.2 O.sub.3 :1.0.+-.P.sub.2 O.sub.5 are disclosed. These compositions have an X-ray diffraction pattern characterized by d spacings at less than about 40 degrees two-theta as measured using copper K-alpha radiation that are substantially as shown in Table 1. The compositions can further comprise a structure-directing agent. Preparation is by admixing an aluminum source, a phosphorus source and 10-100 moles of water per mole of Al.sub.2 O.sub.3 to form a precursor mixture, admixing the precursor mixture with the structure-directing agent to form a reaction mixture, and reacting the reaction mixture under conditions such that an aluminumphosphate composition of the given X-ray diffraction pattern is formed.

Abstract: A method of growing a single crystal of KTiOPO.sub.4 which is a nonlinear optical material is disclosed. Growth of the single crystal of KTiOPO.sub.4 is carried out by melting a KTiOPO.sub.4 material with a flux to produce a melt, then contacting a seed crystal to the melt, and by slowly cooling at a saturation temperature or below. At this time, molar fractions of K.sub.2 O, P.sub.2 O.sub.5 and TiO.sub.2 contained in the melt fall within a region surrounded by six point in a K.sub.2 O-P.sub.2 O.sub.5 -TiO.sub.2 ternary phase diagram of A (K.sub.2 O:0.4150, P.sub.2 O.sub.5 :0.3906, TiO.sub.2 : 0.1944), B (K.sub.2 O:0.3750, P.sub.2 O.sub.5 : 0.3565, TiO.sub.2 : 0.2685), C (K.sub.2 O: 0.3750, P.sub.2 O.sub.5 : 0.3438, TiO.sub.2 : 0.2813), D (K.sub.2 O: 0.3850, P.sub.2 O.sub.5 : 0.3260, TiO.sub.2 : 0.2890), E (K.sub.2 O: 0.4000, P.sub.2 O.sub.5 : 0.3344, TiO.sub.2 : 0.2656), and F (K.sub.2 O: 0.4158, P.sub.2 O.sub.5 : 0.3744, TiO.sub.2 : 0.2098). In addition, K.sub.15 P.sub.13 O.sub.

Abstract: There is provided a catalyst comprising a heteropoly acid, such as phosphotungstic acid, supported on a mesoporous crystalline material, such as M41S. A particular form of this M41S support is designated as MCM-41. There is also provided a method for preparing this catalyst by impregnating the heteropoly acid on the support. There is also provided a process for using this catalyst to catalyze acid catalyzed reactions, such as the isomerization of paraffins and the alkylation of aromatics.

Abstract: Anions of the formula (I):[DA.sub.5 M.sub.30-x O.sub.110-x (M'L).sub.x ].sup.m- (I)in which D is Na.sup.+, Ca.sup.2+; A is P, As, Sb, Si, Ge, or combinations thereof M is W.sup.5+, W.sup.6.alpha., or mixtures thereof; M' is a metallic element from groups 2 to 15 of the periodic table; other than W; L is O.sup.2-, OH.sup.-, H.sub.2 O; x is 0-10; and m is 10-20; selectively react with cations Z.sup.n+ to afford anions of the formula (II):[ZA.sub.5 M.sub.30-x O.sub.110-x (M'L).sub.x ].sup.(m+1-n)- (II)wherein n is 3 or 4; Z=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Y, or Bi, when n=3, and Z=Ce, U, Np, Pu, or Am, when n=4. This reaction may be used for the selective encapsultion of lanthanide or actinide cations, and salts containing anions of formula (II) may be vitrified to form glasses or reduced to form tungsten "bronze" materials suitable for the long-germ storage of radioactive lanthanides or actinides.

Abstract: A deproteinization filler comprises an aggregate of hydroxyapatite fibers having a three dimensional network structure. The mean radius of pores defined by the aggregate is approximately 0.02 .mu.m to approximately 0.08 .mu.m, the specific surface of the aggregate is approximately 25 m.sup.2 /g to approximately 65 m.sup.2 /g and the mean diameter of particles defined by the aggregate is approximately 1 .mu.m to approximately 30 .mu.m. The filler is produced by a given method. The filler may be contained in a throwaway cartridge.

Abstract: The invention describes basic calcium aluminum hydroxy phosphites of the general formulaCa.sub.x Al.sub.2 (OH).sub.2(x+3-y) (HPO.sub.3).sub.y.mH.sub.2 Owhereinx=2-12, ##EQU1## and m=0-12,with the proviso that y.noteq.1, if x=2-8.The compounds according to the invention are particularly suited as stabilizers for halogen-containing polymers, in particular PVC.

Abstract: The present invention provides a composition of matter having the formulaA.sub.x B.sub.1-x V.sub.y C.sub.1-y P.sub.3 O.sub.10-15wherein A is Nb or Ta, B is Sb, C is Ti or Sn, and 0.ltoreq.x,y.ltoreq.1, a composition of matter having the formulaM.sub.z A.sub.x B.sub.1-x V.sub.y C.sub.1-y P.sub.3 O.sub.10-15wherein M is selected from the group consisting of Cu, Ag, Na, K, and Cs, A is Nb or Ta, B is Sb, C is Ti or Sn, and 0.ltoreq.x,y,z.ltoreq.1, a composition of matter having the formulaM.sub.z A.sub.x B.sub.1-x V.sub.y C.sub.1-y P.sub.3-n Si.sub.n O.sub.10-15wherein M is selected from the group consisting of Cu, Ag, Bi, Na, K, Rb, and Cs, A is Nb or Ta, B is Sb or As, C is Ti, Zr, Sn, or Ge, and 0.ltoreq.x,z.ltoreq.1, 0<y.ltoreq.1, and 0.ltoreq.n.ltoreq.2, and conversion processes catalyzed by at least one of the composition.

Abstract: The present invention relates to a solid low temperature phosphorus diffusion source that is an R.sub.2 O.sub.3 /P.sub.2 O.sub.5 compound in which the ratio of R.sub.2 O.sub.3 to P.sub.2 O.sub.5 is 1 to 5 and R is Nd, Eu, Pr, Sm, Ho, Tb, Er, Yb, Tm or Dy. The invention also relates to a method of making the diffusion source, a method of using the diffusion source to evolve P.sub.2 O.sub.5 to dope a silicon wafer, and the doped silicon wafer.

Abstract: The present invention relates to a solid high temperature phosphorus diffusion source that is an R.sub.2 O.sub.3 /P.sub.2 O.sub.5 compound in which the ratio of R.sub.2 O.sub.3 to P.sub.2 O.sub.5 is 1 to 3 and R is La, Y, Ce, Nd, Eu, Pt, Sm, Ho, Tb, Er, Yb, Tm or Dy. The invention also relates to a method of making the diffusion source, a method of using the diffusion source to evolve P.sub.2 O.sub.5 to dope a silicon wafer, and to the doped silicon wafer.

Abstract: A process and novel catalyst for the carbonylation of one or more of alcohols, ethers and ether alcohols to esters and, optionally, to carboxylic acids. The reaction is effected in the vapor state over a solid catalyst comprising a polyoxometalate anion in which the metal is at least one taken from Group V and VI of the Periodic Chart of the Elements complexed with a cation from a member of Group VIIIA of the Periodic Chart of the Elements. Preferably, the catalyst is deposited on a support that is inert to the reaction. The preferred support is silica.

Abstract: Compounds that satisfy the general formula A.sub.1-Y.sup.4+ A.sub.Y.sup.1+ A.sub.Y.sup.3+ V.sub.2-X P.sub.X O.sub.7 exhibit isotropic NTE behavior in the range of normal ambient temperatures. Y is from about 0.0 to about 0.4, and more preferably is about 0.2. X is from about 0.6 to about 1.4, and is more preferably about 1. Particularly suitable NTE compounds have X about 1 and Y about 0. A.sup.4+ is selected from the group consisting of Hf, Zr, Zr.sub.a M.sub.b, Hf.sub.a M.sub.b and mixtures thereof wherein a plus b equals one and M is selected from the group consisting of Ti, Ce, Th, U, Mo, Pt, Pb, Sn, Ge and Si. More preferably, A.sup.4+ is selected from the group consisting of Hf and Zr. A.sup.1+ is selected from the group consisting of the alkali earth metals, and A.sup.3+ is selected from the group consisting of the rare earth metals. Such NTE materials exhibit isotropic negative linear expansion at a temperature below about 100.degree. C.

Abstract: A new class of microporous compositions are described along with a process for preparing them and processes for using them. These compositions have a three-dimensional microporous framework structure of ZnO.sub.2, PO.sub.2 and M'O.sub.2 tetrahedral units, and an intracrystalline pore system. The M' metal is selected from the group consisting of magnesium, copper, gallium, aluminum, germanium, cobalt, chromium, iron, manganese, titanium and mixtures thereof. These molecular sieves are prepared by hydrothermal crystallization of a reaction mixture containing reactive sources of phosphorus, zinc, one or more M' metal, at least one alkali metal and water. This invention also relates to processes using these molecular sieves.

Abstract: The invention describes basic calcium aluminum hydroxy phosphites of the general formulaCa.sub.x Al.sub.2 (OH).sub.2(x+2) HPO.sub.3 .multidot.mH.sub.2 Owhereinx=2-8 andm=0-12and a process for their production.The compounds according to the invention are especially suited as stabilizers for halogen-containing polymers, in particular PVC.

Abstract: The present invention provides a microbicide which comprises a phosphate represented by the following general formula:M.sub.a.sup.1 A.sub.b M.sub.c.sup.2 (PO.sub.4).sub.d.nH.sub.2 Owherein M.sup.1 represents at least one element selected from the group consisting of silver, copper, zinc, tin, mercury, lead, iron, cobalt, nickel, manganese, arsenic, antimony, bismuth, barium, cadmium and chromium, M.sup.2 represents at least one element selected from tetravelent metal elements, A represents at least one ion selected from the group consisting of hydrogen ion, alkali metal ions, alkaline earth metal ions and ammonium ion, n represents a number which satisfies 0.ltoreq.n.ltoreq.6, a and b each represents a positive number and satisfy la+mb=1 or la+mb=2, and when a and b satisfy la+mb=1, c is 2 and d is 3, and when a and b satisfy la+mb=2, c is 1 and d is 2, where 1 is valence of M.sup.1 and m is valence of A.

Abstract: A method for removing ammonia, or ammonia and phosphates from industrial agricultural or household effluents by causing precipitation as magnesium ammonium phosphate by means of a liquid reagent containing magnesium and phosphate ions and an acid. The effluents have more than 1 gle of ammoniacal nitrogen and the pH is adjusted to between 9 and 11 after addition of the liquid reagent.

Abstract: Aluminum phosphate compositions are provided which are characterized simultaneously by high porosity and phosphorous-to-aluminum ratios of approximately 1.0. The high porosity of these compositions is a function of high pore volume coupled with low surface area, resulting in high average pore diameter. These materials have excellent properties as catalysts and catalyst supports. Methods of making the compositions are also provided.

Abstract: A sol-gel process is disclosed for preparing MTiOXO.sub.4 when M is K, Rb, Tl and/or NH.sub.4 and X is P and/or As which involves dissolving suitable compounds of M, Ti and X in stoichiometic amounts in a suitable organic liquid, and then producing crystalline MTiOXO.sub.4 using procedures including hydrolysis, condensation, solidification and pyrolysis. Bulk material and films (e.g., films of KTP on a single crystal silicon substrate) may be produced. Compositions comprising films of said MTiOXO.sub.4 produced by this process are disclosed.

Abstract: Process for treating phosphoric acid for removing heavy metal cations, in particular cadmium, and sludges contained in the acid, characterized in that concentrated phosphoric acid having a low solids content is used and in that the calcium sulfate supersaturation of the phosphoric acid is controlled to form a compound of the formula I:(SO.sub.4).sub.1-x (PO.sub.4).sub.x (H).sub.y Ca.sub.1-67 M;where x is between 0.5.times.10.sup.-2 and 1.times.10.sup.-1 ; y is between 0 and x+.delta.; .delta. indicates the chemical substitution of calcium by other metal cations; and M represents one or more metal cations contained in the initial phosphoric acid, whose total charge is approximately equal to 2.delta.+x-y.The following "Brief Description of Drawings" has been inserted between lines 19 and 20 on page 4 of the specification to comply with 37 CRF 1.74 and MPEP 608.01(f).The sole FIGURE of the Drawings is a flow diagram illustrating one embodiment of the process according to the present invention.

Abstract: A heat resistive phosphate sintered body including a solid solution of R.sub.y Zr.sub.4 Si.sub.x P.sub.6-x O.sub.24 in which O.ltoreq.x.ltoreq.2, 2/3.ltoreq.y.ltoreq.2, R is a combination of one or more of cations having 2-3 valences, and x and y meet an electrically neutral condition, wherein a thermal expansion hysteresis loss is not more than 0.3%, and a dimensional change after a heat cycling in which heating and cooling are repeated between 100.degree. C. and 1,200.degree. C. at 100 times is not more than 1%. A process for producing such a heat resistive phosphate is also disclosed. The process includes the steps of preparing a batch mixture, as a starting material, of (ZrO).sub.2 P.sub.2 O.sub.7, ZrP.sub.2 O.sub.7, RO and/or a phosphate of R in which R is a combination of one or more of cations having two or three valences, and if necessary further SiO.sub.2, calcining, milling and shaping the thus prepared mixture, and firing the thus shaped body, wherein a calcining temperature is not less than 1,400.

Abstract: Olefin polymerization catalysts and processes for preparing and using the catalysts are provided. The catalysts are prepared by forming a particulate gel containing aluminum and magnesium phosphates, calcining the gel and then contacting the calcined gel with a titanium halide and, optionally, an organomagnesium compound.

Abstract: A process for preparing aluminophosphate compounds (and substituted derivatives) of the structural type VFI. This preparation process is characterized in that the speed of increase in temperature of the reaction mixture is greater than 250.degree. C./hour, the total time of heating of the reaction mixture, including the rise in temperature and the plateau heating, being less than one hour. The temperature of the plateau heating is between 100.degree. and 200.degree. C.The synthetic compounds in accordance with the invention possess(a) a general formula approximating to the following:1 Al.sub.2 O.sub.3 0.75-1.25 P.sub.2 O.sub.5 0-0.5 XO.sub.n/2 0-0.05 R y H.sub.2 OwhereX represents a heteroatom chosen from the group consisting of silicon, cobalt, magnesium and zinc;n is the degree of oxidation of the heteroatom X;y, the number of water molecules contained in the said compound, is greater than 0.

Abstract: This invention presents a novel MgAPSO molecular sieve, containing a critical range of magnesium in the sieve framework, which is particularly active for hydrocarbon conversion. The sieve advantageously is incorporated, along with a platinum-group metal, into a catalyst formulation which is useful for isomerization. When utilized in a process for isomerizing a non-equilibrium mixture of xylenes containing ethylbenzene, a greater yield of para-xylene is obtained compared to prior-art processes.

Abstract: Novel molecular sieves are disclosed which are oxides of (a) an alkali metal, an alkaline earth metal and/or ammonium, (b) beryllium, cobalt and/or zinc, and (c) phosphorous, arsenic and/or vanadium, and optionally contain water. These zeolite-like materials, which contain little or no aluminum or silicon, can be made by a novel low temperature process. The molecular sieves are useful as ion exchange resins.

Abstract: A class of new oxide structures containing octahedral molybdenum and tetrahedral phosphorous has been generated using hydrothermal techniques. These materials are produced by the reaction of a molybdenum oxide source with phosphate and any one, or combination of organic cation/alkali-metal cation/organic amine as a templating/mineralizing agent. A reducing agent is necessary to convert the Mo(VI) to a lower valent form and can be either added to the reaction mixture or is provided in the form of one of the reactants.

Abstract: This invention relates to a method for synthesizing a new synthetic composition of ultra-large pore crystalline material which can be used as a sorbent or catalyst component for conversion of organic and inorganic compounds. The crystalline material product of this method exhibits unusually large sorption capacity demonstrated by its benzene adsorption capacity of greater than about 15 grams benzene/100 grams at 50 torr and 25.degree. C., a hexagonal electron diffraction pattern that can be indexed with a d.sub.100 value greater than about 18 Angstrom Units and a hexagonal arrangement of uniformly sized pores with a maximum perpendicular cross section of at least about 13 Angstrom units.

Abstract: Crystalline aluminophosphate compositions having pore windows formed by 18 tetrahedral members are prepared from a forming mixture containing sources of aluminum, phosphorus and optionally, silicon. The forming mixture further contains a directing agent comprising a mixture of quaternary nitrogen compound and amine in a molar ratio of 0.01 to 0.025. The resulting product exhibits greater stability than compositions made from amine directing agent.

Abstract: This invention relates to a new crystalline composition MCM-40, to a method for synthesizing said crystalline composition using diaminocyclohexane as a directing agent and to use of said crystalline composition as a catalyst component for organic compound, e.g. hydrocarbon compound, conversion.

Abstract: This invention relates to a new synthetic composition of ultra-large pore crystalline material and use thereof as sorbent and in catalytic conversion of organic and inorganic compounds. The new crystalline material exhibits unusually large sorption capacity demonstrated by its benzene adsorption capacity of greater than about 15 grams benzene/100 grams at 50 torr and 25.degree. C., a hexagonal electron diffraction pattern that can be indexed with a d.sub.100 value greater than about 18 Angstrom Units and a hexagonal arrangement of uniformly sized pores with a maximum perpendicular cross section of at least about 13 Angstrom units.