Abstract: Method of synthesis for a material made of particles having a core and a coating and/or being connected to each other by carbon cross-linking, the core of these particles containing at least one compound of formula LixM1−yM′y(XO4)n, in which x,y and n are numbers such as 0≦x≦2, 0≦y≦0.6 and 1≦n≦1.5, M is a transition metal, M′ is an element with fixed valency, and the synthesis is carried out by reaction and bringing into equilibrium the mixture of precursors, with a reducing gaseous atmosphere, in such a way as to bring the transition metal or metals to the desired valency level, the synthesis being carried out in the presence of a source of carbon called carbon conductor, which is subjected to pyrolysis. The materials obtained have excellent electrical conductivity as well as very improved chemical activity.

Abstract: The invention is directed to open-framework and microporous solids well suited for use in catalysis and ion exchange. The microporous solids are constructed by using a salt template which can be readily removed without destroying the framework of the micropore. Various microporous solids can be formed having different geometric structures depending upon the templating salt used and the concentration. Examples of two compounds include Na2Cs[Mn3(P2O7)2]Cl and K2.02Cs2.90[Cu3(P2O7)2]Cl2.92. Both compounds have 3-D (Mn,Cu)—P—O frameworks.

Abstract: Electrode active materials, preferably having an olivine structure, of the formula:

Abstract: Electrode active materials, preferably having an olivine structure, of the formula:

Abstract: Electrode active materials comprising lithium or other alkali metals, a transition metal, and a phosphate or similar moiety, of the formula:

Abstract: A process and a composite for removing toxic cations and anions from blood or dialysate is disclosed. The process involves contacting blood or dialysate with a shaped ion exchange composite to remove ammonium and phosphate ions. The composite is a mixture of an anion exchange composition such as zirconia and a microporous cation exchange composition formed into a shaped article and optionally containing a binder such as hydrous zirconium oxide. The microporous cation exchangers are represented by the following empirical formula.

Abstract: A positive electrode active material for a secondary battery contains a spinel lithium manganese composite oxide expressed by a general formula of Lia(MxMn2−x−yAy)O4 where x, y and z are positive values which satisfy 0.4<x, 0<y, x+y<2, and 0<a<1.2. “M” denotes Ni and at least one metal element selected from the group consisting of Co, Fe, Cr and Cu. “A” denotes at least one metal element selected from the group consisting of Si and Ti. The ratio y of A has a value of 0.1<y in case where A includes only Ti. Accordingly, it is possible to acquire a material for the positive electrode of a lithium ion secondary battery, which has a high capacity and a high energy density with a high voltage of 4.5 V or higher with respect to Li.

Abstract: The present invention provides an inexpensive process for the preparation of lithium salts of formula LiX having a desired or required level of purity using lithium chloride and lithium sulfate. In the process of the invention, a lithium salt selected from lithium chloride, lithium sulfate, and combinations thereof is reacted with NaX or KX in a aqueous, semiaqueous, or organic solution and the precipitated salts are removed to obtain the LiX solution of desired purity. Preferably, a semiaqueous solution containing water and an organic solvent is used at some point in the reaction. The process of the invention eliminates the use of highly acidic materials and thus reduces the cost of raw materials and the need for specialized equipment.

Abstract: A dye fixing agent for water-color ink to be contained in the water-color ink accepting layer of an ink jet recording medium having a water-color ink accepting layer formed on a substrate, which is a hydrotalcite compound containing a silicic acid anion and a sulfuric acid ion, or a silicic acid anion as an anion(s) and metal lithium. An ink jet recording medium comprising the dye fixing agent for water-color ink on a substrate. The dye fixing agent for water-color ink provided by the present invention is excellent in the fixability of water-color ink and the ink jet recording medium provided by the present invention is excellent in the resolution, water resistance and light resistance of an image recorded on the medium.

Abstract: The present invention pertains to a composite powder comprising (A) an alkali metal silicate particle having an average particle size of from 1 to 500 &mgr;m; and (B) a water-soluble salt particle having an average particle size of from 0.01 to 50 &mgr;m, of which solubility to water at 20° C. is 1 g/100 g or more, wherein the alkali metal silicate particle has a composition formula in an anhydride form represented by: xM2O.ySiO2.zMeO (I) wherein M stands for Na and/or K; Me stands for Ca and/or Mg; y/x is from 0.5 to 4.0; z/x is from 0 to 1.0; and Mg/Ca in MeO is from 0 to 10, and wherein the composite powder has a (A)/(B) weight ratio of from 1/9 to 99/1; and a detergent composition comprising the composite powder. The composite powder is a composite powder having a remarkably enhanced storage stability of the alkali metal silicate without impairing the ion exchange capacity owned by the alkali metal silicate.

Abstract: A lithium ion secondary cell having a high capacity, improved first charge/discharge efficiency and improved cycle performance is obtainable using as the negative electrode material a lithium-containing silicon oxide powder having the formula: SiLixOy wherein x and y are 0<x<1.0 and 0<y<1.5, with the lithium being fused and partially crystallized.

Abstract: Disclosed is a commercial grade of soluble silicate solutions, clear homogenous and water white essentially free of unreacted silica, made by dissolving in a closed container biogenic silica, preferably rice hull ash, in a strong alkali solution, preferably sodium hydroxide in the presence of an agent, such as an active carbonaceous material, which prevents discoloration of the soluble silicates by absorbing and/or reacting with polyvalent metals, organic materials, and the like, in the biogenic silica as it dissolves in and reacts with the alkali solution. The invention takes advantage of the residue of such active carbonaceous material on the biogenic silica, such as rice hulls, left by commercial energy burning thereof which effectively prevents discoloration. A solid residue results from the method which is an active carbonaceous material including concentrated manganese from the biogenic silica, both of which are valuable commercial products.

Abstract: from Groups 2, 3, 12, 13, or 14 of the Periodic Table. Preferred embodiments include those having where c=1, those where c=2, and those where c=3. Preferred embodiments include those where a ≦1 and c=1, those where a=2 and c=1, and those where a≧3 and c=3. This invention also provides electrodes comprising an electrode active material of this invention, and batteries that comprise a first electrode having an electrode active material of this invention; a second electrode having a compatible active material; and an electrolyte.

Abstract: The present invention includes lithium cobalt oxides having hexagonal layered crystal structures and methods of making same. The lithium cobalt oxides of the invention have the formula LiwCo1−xAxO2+y wherein 0.96≦w≦1.05, 0≦x≦0.05, −0.02≦y≦0.02 and A is one or more dopants. The lithium cobalt oxides of the invention preferably have a position within the principal component space defined by the relationship axi+byi≦c, wherein xi={right arrow over (S)}i&Circlesolid;{right arrow over (P)}c1; yi={right arrow over (S)}i&Circlesolid;{right arrow over (P)}c2; the vector {right arrow over (S)}i is the x-ray spectrum for the LiwCo1−xAxO2+y compound; the vectors {right arrow over (P)}c1 and {right arrow over (P)}c2 defining the principal component space are determined by measuring the x-ray powder diffraction values {right arrow over (S)}i between 15° and 120° using a 0.

Abstract: The invention describes a process for preparing P zeolites in which aluminate and silicate solutions are reacted in the presence of a P-zeolite seed.

Abstract: The invention describes a process for preparing P zeolites in which aluminate and silicate solutions are reacted in the presence of a P-zeolite seed.

Abstract: An aqueous solution with a pH of greater than 5, preferably of at least 6.5, can be used in an ion-exchange process, in particular a process for the manufacture of a zeolite. This aqueous solution comprises metal cations, such as zinc, and an agent for complexing the metal cations, such as citric acid or a salt of this acid. The proportion of free cations in solution represents from 0.1% to 99%, preferably from 1 to 30%, of the total amount of the metal in the solution. The invention also relates to a process for the manufacture of zeolites X or A employing such an aqueous solution and the use of the zeolites thus obtained for separating, purifying or converting one or more constituents of a gas stream, such as air, synthesis gases or hydrocarbons, in particular olefins, by employing an adsorption process, in particular a PSA, VSA or TSA.

Abstract: Disclosed is a carbon dioxide gas absorbent containing lithium silicate reacting with a carbon dioxide gas to form lithium carbonate and represented by the general formula, LixSiyOz, where x, y, z are integers meeting the requirement of x+4y−2z=0. The lithium content x in the general formula should desirably be at least 4.

Abstract: Crystalline microporous rare earth silicates are provided. These microporous compositions have a three dimensional framework structure of at least silicon tetrahedral oxide units and at least one M oxide unit. M is a rare earth element. Optionally, the microporous compositions may contain as part of the framework an M′ element having a valence of +2, +3, +4 or +5 such as zinc (+2), iron (+3), zirconium (+4) and tantalum (+5). The composition is represented by the empirical formula: An(M1−zM′z)wSi1−yGeyOx where A is a cation such as sodium and “n”, “z”, “w”, “y” and “x” are the mole fractions of the various elements.

Abstract: Colloids comprising amorphous borosilicate particles, wherein said borosilicate particles are not borosilicate glass; are described and claimed. These colloids have been found to be useful in aqueous systems, specially in papermaking.

Abstract: The present invention relates to trioctahedral phyllosilicates 2:1 of a stevensite or kerolite type containing fluorine, fluorinated in synthesis in an acid medium in the presence of hydrofluoric acid and/or another source of fluoride anions. The invention also relates to a method of preparation to obtain said phyllosilicate. The existence of gaps enables adjustable quantities of cations to be incorporated in the gaps and hence the exchange capacity of said solids to be modulated. These phyllosilicates, raw from synthesis or after post-synthesis modification, may be incorporated in the composition of catalysts used to convert hydrocarbons, in particular for hydrocracking.

Abstract: The invention comprises a borosilicate retention aid composition and a method for improving the production of paper by addition of the borosilicate. The borosilicate may be utilized in conjunction with a high molecular weight synthetic flocculant and/or starch, with or without the addition of a cationic coagulant. The borosilicate material is preferably a colloidal borosilicate. Methods for the preparation of the borosilicate material are disclosed.

Abstract: The invention relates to a synthetic magnesium silicate having a layered crystalline structure, to a process for its preparation and to its use.

Abstract: The present invention relates to a compacted sodium silicate is provided having a molar ratio SiO2:Na2O from 1.6 to 3.3, characterized in that the silicate has the following properties: a bulk density of above 500 g/l, a porosity of above 190 ml/kg, and a mechanical strength corresponding to a dust percentage of below 40 wt %. Also provided is a process for preparing such silicate comprising the steps of: spray-drying an aqueous solution of sodium silicate with a molar ratio SiO2:Na2O from 1.6 to 3.3, applying an outlet temperature above 114° C., applying a water glass solution to the spray-dried powder, subjecting the water glass treated powder to a compacting step, applying a pressure below 100 bar, and crushing the resulting flakes having a thickness of above 4 mm to obtain the compacted sodium silicate.

Abstract: The disclosure relates to the forming mineralized coatings on metal surfaces and to methods of forming such coatings. The coating can include a wide range of compounds and normally at least a portion of the coating corresponds to an amorphous phase. The coating and method are particularly useful in providing a corrosion resistant coating or film upon a metallic surface. This aspect of the disclosure involves the formation of a corrosion resistant “mineralized” layer of tailored composition upon a metal substrate.

Abstract: Incorporation of neutral water soluble inorganic salts into a precipitated silica improves the filler dispersion in a compounded rubber, reduces rolling resistance (hysteresis), and improves processability. These properties are achieved without loss of the expected reinforcement effect due to the substitution of inorganic salt for SiO2 in the silica. The properties are seen when a variety of silanes and processing aids are added to the silica.

Abstract: An amorphous mineralized coating upon an iron containing surface wherein the amorphous mineralized coating has a formula A.sub.x B.sub.y O.sub.z --nH.sub.2 O wherein A comprises iron and B comprises silicon and the values of x, y and z are greater than zero; wherein the amorphous mineralized coating comprises an amorphous phase and inorganic complex oxide crystals.

Abstract: The disclosure relates to the forming mineralized coatings on metal surfaces and to methods of forming such coatings. The coating can include a wide range of compounds and normally at least a portion of the coating corresponds to an amorphous phase. The coating and method are particularly useful in providing a corrosion resistant coating or film upon a metallic surface. This aspect of the disclosure involves the formation of a corrosion resistant "mineralized" layer of tailored composition upon a metal substrate.

Abstract: A method for producing a crystalline inorganic builder having the following composition in its anhydrous form: xM.sub.2 O.ySiO.sub.2.zMeO, wherein x, y and z are numerical values satisfying the following relationships: y/x is 1.0 to 4.0, z/y is not more than 1.0, M stands for Na and K, K/Na is 0.01 to 2.0, and Me stands for Ca and/or Mg, the method comprising the steps of (a) adding water, a Na-containing compound, a K-containing compound, and at least one member of Ca-containing compounds and Mg-containing compounds to silica sand, to give a mixture; (b) subjecting the resulting mixture to a hydrothermal treatment; and (c) baking the resulting treated mixture. Also, a method for producing a crystalline inorganic builder having the following composition in its anhydrous form: xM.sub.2 O.ySiO.sub.2, wherein x and y are numerical values satisfying the following relationships: y/x is 1.0 to 4.0, M stands for Na and K, K/Na is 0.01 to 2.

Abstract: The invention relates to a process for the preparation of crystalline sodium silicates having a sheet structure and high .delta. phase content from water glass, which has been prepared hydrothermally, by dehydration of the water glass and subsequent crystallization at elevated temperature, which comprises treating the water glass at temperatures of from 50 to 140.degree. C. prior to dehydration.

Abstract: A hydrothermal reaction which dissolves the amorphous silica and the crystalline silica impurities contained in a recovered, naturally occurring montmorillonite clay, and subsequently converts the dissolved silicas into a dioctahedral and/or trioctahedil smectite clay. The dissolution of silica is accomplished by adjusting the pH of an aqueous slurry of the recovered clay to a value of about 8.5 to about 10.0, preferably about 9.0 to about 9.5, at a temperature of at least about 150.degree. C., preferably about 180.degree. C. to about 250.degree. C., more preferably about 190.degree. C. to about 235.degree. C. Dissolved silica reacts with stoichiometric amounts of aluminum and/or magnesium and/or sodium added to the slurry, while at a temperature of at least about 150.degree. C., preferably about 185.degree. C. to about 250.degree. C.

Abstract: A fire resistant liquid and a process for the preparation thereof characterized in reacting granulated potassium hydroxide, powdered sodium carbonate, lumps of metallic silicon and water. A fireproof building material molded by applying a viscous liquid of the fire resistant liquid mixed with bentonite and fibers on one or both sides of wood-, paper-, metal- and composite boards, and a fireproof building material molded by laminating an incombustible cotton plate to a base plate through a compounding mixture of the fire resistant liquid with bentonite and Chinese cotton are prepared. A fire resistant adhesive is prepared by mixing the fire resistant liquid with bentonite, Chinese cotton and BENGEL 31.

Abstract: Novel magnesiosilicate compounds for use in detergent compositions and as water softeners have a calcium binding capacity of at least 10 mg CaO per gram, a magnesium binding capacity of at least 10 mg MgO per gram and a calcium binding rate of no more than 300 seconds, all at room temperature. The compounds have a stuffed silica polymorph-related structure or a layered structure with a broad X-ray powder diffraction peak at a d-spacing of between 11 and 17 .ANG.. The compounds have an anhydrous composition M.sub.a Mg.sub.b Al.sub.c Si.sub.1-(b+c) O.sub.d, where M--alkali, 0.0<a<2.0, 0.0<b<0.7, 0.0.ltoreq.c.ltoreq.0.3, 1.15<d<3.0, c<b, and partial substitution of M, Mg, Al and Si is permitted.

Abstract: The invention relates to a process for the preparation of crystalline sodium silicates having a sheet structure and high .delta. phase content from water glass, which has been prepared predominantly hydrothermally, by dehydration of the water glass and subsequent crystallization at elevated temperature, wherein the water glass is a mixture of water glass prepared hydrothermally and tank furnace water glass, and also to its use.

Abstract: The method for producing a crystalline, inorganic ion exchange material having the following composition: xM.sub.2 O.ySiO.sub.2.zMeO, wherein x, y and z are numerical values satisfying the relationships of y/x=0.5 to 2.1, preferably 0.5 to 2.0, and z/y=0.001 to 1.0; M stands for Na and K, wherein K/Na is in the range from 0.01 to 1.2; and Me stands for Ca and/or Mg, the method including the steps of adding 1 to 85 parts by weight of water to 100 parts by weight of cullets, wherein the cullets have the following compositon: xM.sub.2 O.ySiO.sub.2 .multidot.zMeO, wherein x, y, z, M, and Me are defined as above, and then baking the resulting mixture.

Abstract: Pulverulent detergent compositions, particularly suitable for washing and dishwashing machines, include a surfactant and a builder therefor, such builder comprising an alkali metal silicate advantageously having a SiO.sub.2 /M.sub.2 O molar ratio ranging from about 1.6 to 3.5, at least 30% and preferably at least 50% of the silicon atoms of which being in the Q.sub.2 and Q.sub.3 configurations, or such builder comprising said alkali metal silicate sorbed onto a particulate inert support substrate. Also, detergent compositing comprising (a) an aqueous solution of an alkali metal silicate having an SiO.sub.2 /M.sub.2 O molar ratio ranging from about 1.

Abstract: Homostructured, cation exchanged, layered compositions containing mixed onium and alkali metal, alkaline earth metal, protonated hydronium ions and mixtures thereof are described. Particulate concentrates formed by intercalation of a polymer component into the galleries of the layered inorganic and organic homostructured layered cation exchange composition and to the use of the particulate concentrates for the preparation of cured polymer-inorganic nanolayer hybrid composite compositions are described. In the most preferred embodiment of the invention the layered inorganic composition is selected from the family of 2:1 layered silicate clays.

Abstract: Provided is a mesopore material and the manufacturing method thereof characterized by having uniform diameter of each pore as well as a high crystallographic regularity, comprising primary particles having a small axe with uniformity, allowing for synthesizing the primary particles with the size freely controlled, and allowing for simple manufacturing at a reduced cost. The mesopore material comprising: pores having a diameter in a range of 2 to 10 nm; and a primary particle having a major axe in a range of 10 nm to 1 .mu.m. The diameter range is defined at a maximum peak in a pore distribution curve, and 75% or more of the pores is in a diameter range of -40% to +40% of the pore diameter at the maximum peak. Further provided is a laminar silicic acid composed of the uninvertible tetrahedral sheet and has a uniform shape and size. Also provided is a laminar silicic acid salt composed of the uninvertible tetrahedral sheet and has a uniform shape and size.

Abstract: A microwave-dried amorphous alkali metal silicate detergent builder is provided characterized by a surface area of at least 20 m.sup.2 /gram and a water content of at least about 13%, by weight. The microwave-dried silicate provides effective complexation with hardness ion in wash water and more rapid solubility than conventional spray-dried silicate powders. The microwave-dried silicate can function as an efficient builder in laundry detergent compositions and over a broad range of laundry detergent applications.

Abstract: A method for fabricating a porous composite oxide is provided. The method includes the steps of: (a) slowly mixing a solution including a silicon oxide source and a solution including an aluminum oxide source; (b) adding hydrochloric acid to the mixed solution prepared in said step (a) to obtain a sol; and (c) adding sodium hydroxide to said sol, reacting the obtained resultant at room temperature for 30 minutes to 12 hours, and drying the resultant. The porous composite oxide has an abundance of fine pores and the distribution of pore size is relatively uniform, so that the porous composite oxide is suitable for a carrier.

Abstract: A process for producing a particulate amorphous alkali metal silicate having a molar ratio of M.sub.2 O to SiO.sub.2 of 1:1.5 to 1:3.3 bya) spray-drying an aqueous mixture of amorphous alkali metal silicate,b) impregnating the spray-dried amorphous alkali metal silicate with an aqueous dispersion or solution of detergent composition components containing at least one organic component, andc) optionally drying the impregnated amorphous alkali metal silicate.

Abstract: A silicon dioxide tetrahedron sheet having a specific morphology with the pseudomorphs of the starting raw material of clay minerals for the sheet is prepared, and this is reacted with an alkylonium salt whereby a desired number of the silicon dioxide tetrahedrons are removed from the sheet by the action of the micelles of the alkylonium salt formed on the surface of the sheet to thereby form mesopores in the sheet. The mesopore material of the sheet has phyllo-structured 6-membered skeletons as connected to each other, in which each one phyllo-structured 6-membered skeleton is formed by connecting 6 silicon dioxide tetrahedrons together, and its mesopores are formed by removing a desired number of the silicon dioxide tetrahedrons from the sheet.

Abstract: A method for producing a crystalline, inorganic ion exchange material having the following composition: x.sub.1 K.sub.2 O.x.sub.2 Na.sub.2 O.ySiO.sub.2. zMeO, wherein x.sub.1, x.sub.2, y and z are numerical values satisfying the following relationships: y/(x.sub.1 +x.sub.2)=1.0 to 2.1, z/y=0 to 1.0, x.sub.1 /x.sub.2 =0.01 to 2.0, and Me stands for Ca and/or Mg, the method including the steps of adding and blending one or more alkali metal compounds, or one or more alkali metal compounds and one or more alkaline earth metal compounds in cullets having a composition of SiO.sub.2 /Na.sub.2 O=1.5 to 4.2, and baking the resulting mixture.

Abstract: The disclosure relates to the forming mineralized coatings on metal surfaces and to methods of forming such coatings. The coating can include a wide range of compounds and normally at least a portion of the coating corresponds to an amorphous phase. The coating and method are particularly useful in providing a corrosion resistant coating or film upon a metallic surface. This aspect of the disclosure involves the formation of a corrosion resistant "mineralized" layer of tailored composition upon a metal substrate.

Abstract: The disclosure relates to the forming mineralized coatings on metal surfaces and to methods of forming such coatings. The coating can include a wide range of compounds and normally at least a portion of the coating corresponds to an amorphous phase. The coating and method are particularly useful in providing a corrosion resistant coating or film upon a metallic surface. This aspect of the disclosure involves the formation of a corrosion resistant "mineralized" layer of tailored composition upon a metal substrate.

Abstract: Fiber-reinforced geopolymeric resin having a mole ratio of SiO.sub.2 :Al.sub.2 O.sub.3 of at least equal to 6, and preferably at least equal to 10, adheres well to both concrete and steel, and is used to protectively cover infrastructures formed of steel-reinforced concrete and the like.

Abstract: A process suitable for producing high purity alkaline earth fluoride product is disclosed which involves (a) mixing (i) MgO, CaO, BaO, Mg(OH).sub.2, Ca(OH).sub.2, and/or Ba(OH).sub.2, (ii) NaOH, KOH and/or NH.sub.4 OH, and (iii) water, to form an aqueous slurry having a temperature of at least 20.degree. C. and an aqueous phase pH of at least 13; (b) adding fluosilicic acid, optionally adding additional water and optionally adding additional NaOH, KOH and/or NH.sub.4 OH to the slurry of (a) at a rate which maintains an aqueous phase pH of 11 or above, and in an amount to provide a molar ratio of Si: (Mg, Ca, and Ba) of at least 1:3.3, a molar ratio of (Na, K, and NH.sub.4):Si of at least 2:1, and a molar ratio of water:Si of at least 20:1, and to obtain a precipitate comprising an alkaline earth fluoride (MgF.sub.2, CaF.sub.2 and/or BaF.sub.2), and an aqueous solution of a soluble silicon anionic compound; and (c) recovering the alkaline earth fluoride product.

Abstract: A tablet composition containing 2% to 100% by weight of amorphous crystalline or partly crystalline layer-form sodium silicates corresponding to the formula Na.sub.2 Si.sub.x --O.sub.2x+1.yH.sub.2 O wherein x is a number of 1.9 to 4 and y is a number of 0 to 20, with the proviso that the tablet composition only contains water in a quantity such that the maximum theoretical water-binding capacity of the components of the composition is not exceeded.

Abstract: The invention relates to a process for preparing sodium disilicate in the .beta. form having a high ion-exchange capacity and a molar ratio Na.sub.2 O:SiO.sub.2 of about 1:2 from a silicate source and sodium hydroxide solution at elevated temperature, with the product formed being separated off by filtration, wherein the product is further heat treated at from 450.degree. to 780.degree. C. and/or is pressed to form compact parts.

Abstract: A new family of crystalline molecular sieves have been synthesized. These compositions have a microporous structure of ZrO.sub.3 octahedral units, and at least one of SiO.sub.2 tetrahedral units and GeO.sub.2 tetrahedral units. Optionally, the molecular sieves contain M metals such as titanium, niobium, or tin. These novel molecular sieves are prepared hydrothermally from a reaction mixture composed of reactive sources of the components. Additionally, these molecular sieves are useful for the selective adsorption of ammonium ions.