Title of Invention	A PROCESS FOR THE PREPARATION OF LAYERED DOUBLE HYDROXIDE FROM HOMOGENEOUS NANOBINARY OR TERNARY METAL OXY/HYDROXIDE OF LDH
Abstract	The present invention relates to a process for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH. The process involves preparing LDH with high surface area and 1-10 nm size by aerogel procedure.The process steps are: homogenization of metal organic precursors in solvent mixture, controlled hydrolysis, gelation, hydrothermal treatment and finally supercritical drying of solvent finally adding anions to free flowing powder of LDH to self assemble into normal layered double hydroxides.

Title of Invention

A PROCESS FOR THE PREPARATION OF LAYERED DOUBLE HYDROXIDE FROM HOMOGENEOUS NANOBINARY OR TERNARY METAL OXY/HYDROXIDE OF LDH

Abstract

The present invention relates to a process for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH. The process involves preparing LDH with high surface area and 1-10 nm size by aerogel procedure.The process steps are: homogenization of metal organic precursors in solvent mixture, controlled hydrolysis, gelation, hydrothermal treatment and finally supercritical drying of solvent finally adding anions to free flowing powder of LDH to self assemble into normal layered double hydroxides.

Full Text	Field of the invention The present invention relates to aprocess for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH.In particular it relates to a process for preparing and self-assembly of nanobinary and ternary metal oxy/hydroxides with high surface area and 1-10 nm size by aerogel procedure, involving homogenization of metal organic precursors in solvent mixture, controlled hydrolysis, gelation, hydrothermal treatment and finally supercritical drying of solvent. During the self-assembly, the nano materials can be modulated into thin films, nano fibers, membranes, layered structures embedded with intercalated anions comprising of inorganic and organic anions selected from carbonates, phosphates, chromates, ibuprofen, dichlorofenec, salicylic acid, tartaric acid, dyes, and any other similar anions. These self- assembled materials find applications as catalysts, gene reservoirs, controlled drug release, solar energy harvesters. Background of the invention Nano materials have generated unprecedented interest due to their unusual physical and chemical properties with wide and divergent applications in optics, electronics, magnetics, mechanics and catalysis. Nanocrystalline metal oxides exhibit unparalleled destructive adsorption properties of acid gases, polar organics, and even chemical/biological warfare agents. Due to high surface area, these nanostructured solid materials display good catalytic activity in isomerisation, alkylation, reforming and dehydrohalogenation reactions. Generally, aerogel samples are prepared by supercritical drying of a gel from a sol-gel reaction. The aerogel has a specific high surface area with low density. Due to its physical characteristics, aerogel sample is useful as a catalyst or as a carrier for a catalyst. LDHs, which consist of alternating cationic M111-X M"'X (0H)2X+ and anionic An-.zH20 layers have received much attention in recent times in view of their potential applications as catalysts, adsorbents, biomateriais for controlled drug delivery and gene reservoirs. Reference is made to Nanostnictured Materials, 1999, 11, 1091 wherein nano particles of Zinc oxide and alumina were prepared independently by chemical arrested precipitation and then converted into nanocomposites by wet mixing. The inherent disadvantage of this protocol is the development of non-homogeneous material. Reference is made to Journal of Solid State Chemistry, 2002, 165, 193 wherein binary oxides like titanium dioxide and tin oxide are prepared by stearic acid method wherein particle size range from 10-15 nanometers. The drawback is the system is non- homogeneous. Reference is made to Chemistry of Materials, 2002, 14, 2922 wherein binary alumina and magnesium oxides were prepared by sol-gel method. The ratios of the alumina and magnesium oxides were not related to the normal hydrotalcites. The drawback is the system is non- homogeneous. Reference is made to Nature, 2000, 403, 65 wherein the homogeneous nanobinary barium oxide and alumina were synthesized by reverse microemulsion technique. The particle size ranges from 3-10 nanometers. The drawback is use of expensive protocol. Reference is made to Microporous and Mesoporous Materials, 2000, 39, 229 wherein the nano layered double hydroxides were prepared by sol-gel method. The drawbacks are the size of the particles are high, ranging from 300-600 nanometers and the surface area of the samples lower ranging from 240-270 m2/g. Reference is made to Chemistry of Materials, 2002, 14, 4286 wherein nanolayered double hydroxides with uniform crystal size were prepared by co-precipitation in colloid mill and aging for 100°C for 13 h. The drawback is that the particle size obtained in this method is about 60-80 nanometers. Reference is made to Journal of American Chemical Society, 2000, 122, 3530 wherein the zeolite nanoparticles assembles into thin films, membranes, or fibers. Reference is also made to Angewandte Chemie, 2002, 41, 1188 wherein the quasi-spherical zinc oxide nanoparticles assemble into nanorods. Objects of the invention The main object of the present invention is to provide a process for preparing homogeneous nanobinary and ternary metal oxy/hydoxides. It is another object of the invention to provide a process for preparing nano materials with high surface area and low particle size. It is another object of the invention to provide a process for the preparation of nano oxy/ hydroxide material with applications as catalysts and adsorbents. Yet another object of the invention is to provide a process for preparing nanomaterials by self-assembly with anions leading to the formation of normal LDHs with applications as biomaterials for controlled drug delivery and gene reservoirs, preparation of thin films and membranes. Summary of the invention The present invention provides a process for the synthesis of homogeneous nanobinary oxy/hydroxides composed of Mg2+ and Al3+, and nanoternary oxy/hydroxides comprising of Ni, Mg and Al by the aerogel protocol for the first time. Accordingly, the present invention provides a process for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH with high surface area and 1-10 nm particle size by an aerogel protocol, comprising i) hydrolysing a metal alkoxides or metal acetylacetonates in a solvent mixture selected from alcohols and hydrocarbons, by controlled addition of deionised water or a mixture thereof with alcohols, aging for 6 to 16 hours, ii) followed by hydrothemnal treatment, iii) supercritical drying to obtain a free flow powder of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH, iv) adding anions selected from the group consisting of carbonates, phosphates, chromates, ibuprofen, salicylic acid and tartaric acid to self assemble the free flowing powder into normal layered double hydroxides. In one embodiment of the invention, the metal in the metal alkoxides/acetylacetonates is selected from the group consisting of bivalent metals ions comprising essentially of Mg^"^, and trivalent metal ions consisting essentially of Al2+. In another embodiment of the invention, the bivalent metal ions comprise Mg2+ and one or more bivalent metal ions selected from the group consisting of Ni2+, Cu2+,Co2+, Zn2+, Fe2+ and Mn2+ ions. In yet another embodiment of the invention, the trivalent metal ions comprise AP+, and one or more trivalent metal ions selected from the group consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3+, V3+,Ti3+, La3+ and In3+ ions. In a further embodiment of the invention, the ratio of bivalent to trivalent metal ions is in the range of from 1-5. In another embodiment of the invention, the hydrothermal treatment is carried out at a temperature in the range of 100 to 300°C and pressure in the range of 50 to 150atm. In an embodiment of the present invention, the hydrolysis comprises homogenization of metal precursors in hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric amount of deionised water. In an embodiment of the present invention, the metal alkoxides used are selected from the group consisting of methoxide, ethoxide, isomers of propoxide, butoxide and pentoxide. In another embodiment of the present invention, the ratio of bivalent to trivalent metal ions is 2 to 3. In an embodiment of the present invention, the solvent mixture used is selected from a mixture of any of hexane, toluene, xylene, methanol, ethanol and butanol. In an embodiment of the present invention, the aging is preferably effected in a time period of 10 to 12 hours. In another embodiment of the present invention, the reaction mixture is hydrothermally heated at a temperature of 1°C per minute to a temperature in the range of 260 to 280°C, and kept for 5 to 10 minutes under higher pressures from 60 to 120atm. In still another embodiment of present invention, the solvent mixture is vented out at super critical conditions to obtain a free flow of nano LDH. In yet another embodiment of the present invention, the recovered solvent free aerogel is dried overnight about 120°C to remove the traces of solvent. In yet another embodiment of the present invention, the surface areas of homogeneous nanobinary and ternary materials range from 500-700 m2/g. In yet another embodiment of the present invention, particle size of the homogeneous nanobinary and ternary materials ranges from 1-10 nm. In still another embodiment of the present invention, the nanoparticles selfassemble on treatment with sodium carbonate/ phosphate/ chromate/ ibuprofen, dicholorofenec solution at room temperature to normal layered double hydroxides. In a further embodiment of the invention, the self assembled nanostructured LDH is obtained in the form of a hexagonal, fibrous, membrane or thin film. The present invention also provides a process for the preparation of selfassembled layered double hydroxides made of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH of high surface area and 1-10 nm particle size, comprising hydrolyzing a metal aikoxide or metal acetylacetonate in a solvent mixture selected from alcohols and hydrocarbons, by controlled addition of deionised water or a mixture thereof with alcohols, aging for 6 to 16 hours, followed by hydrothermally treating and finally supercritical drying to obtain a free flow powder of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH, adding anions selected from the group consisting of carbonates, phosphates, chromates, ibuprofen, salicylic acid and tartaric acid to self assemble the free flowing powder into normal layered double hydroxides. In one embodiment of the invention, the metal in the metal alkoxides/acetylacetonates is selected from the group consisting of bivalent metals ions comprising essentially of Nig2"1", and trivalent metal ions consisting essentially of A13+. In another embodiment of the invention, the bivalent metal ions comprise Mg2 and one or more bivalent metal ions selected from the group consisting of Ni2+, Cu2+, Co2+, Zn2+, Fe2+ and Mn2* ions. In yet another embodiment of the invention, the trivalent metal ions comprise AP+ and one or more trivalent metal ions selected from the group consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3, V3+, Ti3+, La3+ and In3 ions. In a further embodiment of the invention, the ratio of bivalent to trivalent^ metal ions is in the range of from 1-5. In another embodiment of the invention, the hydrothermal treatment is carried out at a temperature in the range of 100 to 300°C and pressure in the range of 50 to ISOatm. In an embodiment of the present invention, the hydrolysis comprises homogenization of metal precursors in hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric amount of deionised water. In an embodiment of the present invention, the metal alkoxides used are selected from the group consisting of methoxide, ethoxide, isomers of propoxide, butoxide and pentoxide. In another embodiment of the present invention, the ratio of bivalent to trivalent metal ions is 2 to 3. In an embodiment of the present invention, the solvent mixture used is selected from a mixture of any of hexane, toluene, xylene, methanol, ethanol and butanol. In an embodiment of the present invention, the aging is preferably effected in a time period of 10 to 12 hours. In another embodiment of the present invention, the reaction mixture is hydrothermally heated at a temperature of 1 er minute to a temperature in the range of 260 to 280°C, and kept for 5 to 10 minutes under higher pressures from 60 to 120atm. In still another embodiment of present invention, the solvent mixture is vented out at super critical conditions to obtain a free flow of nano LDH. In yet another embodiment of the present invention, the recovered solvent free aerogel is dried overnight about 120°C to remove the traces of solvent. In yet another embodiment of the present invention, the surface areas of homogeneous nanobinary and ternary materials range from 500-700 m2/g. In yet another embodiment of the present invention, particle size of the homogeneous nanobinary and ternary materials ranges from 1-10 nm. In still another embodiment of the present invention, the nanoparticles selfassemble on treatment with sodium carbonate/ phosphate/ chromate/ ibuprofen, dicholorofenec solution at room temperature to normal layered double hydroxides. In a further embodiment of the invention, the self assembled nanostructured LDH is obtained in the form of a hexagonal, fibrous, membrane or thin film. Detailed Description of the Invention The novelty of the present invention relates to a process for preparing and selfassembly of nanobinary and ternary metal oxy/hydroxides of Mg-Al binary (Mg/Al ratios 2:1 and 3:1) and Ni-Mg-Al ternary systems [(Mg+Ni)/Al ratios (1.3+0.7): 1 and (1.9+1.1): 1] by aerogel procedure, involving homogenization of metal organic precursors in solvent mixture, controlled hydrolysis, gelation, hydrothermal treatment and finally supercritical drying of solvent. The novelty of the present invention provides a process for manufacturing of homogeneous nanobinary and ternary metal oxy/hydroxides by aerogel method with an increased surface area. The self-assembly of the nano metal oxy/ hydroxides when mediated by anion forms normal layered double hydroxides. These self- assembled materials finds applications as catalysts, gene reservoirs, controlled drug release, solar energy harvesters. The nanobinary and ternary metal oxy/hydoxides have particle size ranging from 1-10 nanometers and high surface area in the range of 500-700 m2/g. Preferred compositions are made from alkoxides and acetylacetonates of the desired metals. The nanobinary and ternary metal oxy/hydoxides prepared in the present invention have an excellent self-assembling property and can be modulated into thin films, fibers, membranes, when mediated by anions selected from inorganic and organic anions such as carbonates, phosphates, chromates, ibuprofen, dichlorofenec, salicylic acid, tartaric acid, dyes, and any other similar anions. The unprecedented self-assembly of these nanoparticles driven by anion to normal LDH, helps in controlled drug release, solar energy harvester, gene reservoir. The process of the present invention generally comprises an aerogel protocol, comprising hydrolysis of metal alkoxides /acetylacetonates selected from bivalent metals ions comprising Mg2+ or any other metals consisting of Ni2+, Cu2+, Co2+, Zn2+, Fe2+ and Mn2+ ions and trivalent metal ions selected from A13+ and optionally other metals consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3^, V3+, Ti3+, La3+ and In3+ ions in different ratios of M(II)/M(III) ranging from 1-5 in a solvent mixture selected from alcohols /hydrocarbons, by controlled addition of deionised water/their mixtures with alcohols, aging for 6 to 16 hours, followed hydrothermal treatment at temperatures ranging from 100 to 300 °C and pressures ranging from 50 to 150 atm and finally supercritical drying to obtain a free flow powder and the nanostructured LDH self assembled by the addition of anions selected from carbonates, phosphates, chromates, ibuprofen, salicylic acid, tartaric acid, etc, into normal layered double hydroxides in hexagonal, fibrous, membrane or thin film. Hydrolysis preferably involves homogenization of metal precursors in hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric amount of deionised water. Metal alkoxides used are selected from methoxide, ethoxide, isomers of propoxide, butoxide and pentoxide. Preferred ratio of bivalent and trivalent metal ions is 2 to 3. The solvent mixture used is selected from hexane, toluene, xylene, methanol, ethanol, butanol etc., and aging is preferably done for 10 to 12 hours. The reaction mixture is hydrothermally heated with the ramping of temperature 1 °C per minute to 260 to 280 °C, and kept for 5 to 10 minutes under higher pressures from 60 to 120 atm. The solvent mixture is vented out at super critical conditions to obtain a free flow of nano LDH. The recovered solvent free aerogel is dried overnight about 120 °C to remove the traces of solvent. The surface areas of homogeneous nanobinary and ternary materials range from 500-700 m2/g and particle size ranges from 1-10 nm. It is observed that the nanoparticles self-assemble on treatment with sodium carbonate/ phosphate/ chromate/ ibuprofen, dicholorofenec solution at room temperature to normal layered double hydroxides. The following examples are given by way of illustration of the present invention and therefore should not be constructed to limit the scope of invention. Example 1 Preparation of nanobinary Mg/Al (2/1) system In aerogel method, magnesium turnings (2.4g, 0.1M) were allowed to react with freshly dried methanol (100 mL) under argon flow by stirring. Dry toluene (300 mL) was added to the resultant magnesium methoxide solution and continued stirring for2 hours. Aluminum isopropoxide (10.235 g, 0.05M) (for 2:1 system) was then added to the resultant solution and stirred for 2 more hours. Then stoichiometric amount of deionised water (4.85 mL) was added using capillary addition pump over a period of 0.5 h. This solution was kept under stirring overnight at room temperature. The pH of the slightly milky white solution was found to be >7. The resultant solution was placed in an autoclave, heated in 4 hours to 265 °C with a resultant pressure of 60-80 atm, kept for 10 min, vented to obtain an aerogel material and further dried at 120 °C to remove the traces of solvent. Example 2 Preparation of nanoternary Ni+Mg/Al ((0.7+1.3)/!) system In aerogel method, magnesium turnings (1.56 g, 0.13M) were allowed to react with freshly dried methanol (65 mL) under argon flow. Under vigorous stirring, dry toluene (195 mL) was added to the resultant magnesium methoxide solution and stirred for 2 hours. Aluminum isopropoxide (20.475 g, 0.1M) was then added to the resultant solution and stirred for 2 more hours. Nickel acetylacetonate (17.99 g, 0.07 M) (for 2:1 system) was added to the resultant solution and stirred for 2 more hours. Then stoichiometric amount of deionised water (10.26 mL) was added using capillary addition pump over a period of 0.5 hours. This solution was kept under stirring overnight at room temperature. The pH of the slightly milky white solution was found to be >7. The resultant solution was placed in an autoclave, heated to 265 °C in 4 hours with a resultant pressure of 120-130 atm, kept for 10 minutes, vented to obtain an aerogel material and further dried at 120 °C to remove the traces of solvent. Example 3 Preparation of nanobinary Mg/Al (3/1) system In aerogel method, magnesium turnings (1.8 g, 0.075 M) were allowed to react with freshly dried methanol (75 mL) under argon flow. Under vigorous stirring, dry toluene (225 mL) was added to the resultant magnesium methoxide solution and stirred for 2 hours. Aluminum isopropoxide (5.12 g, 0.025M) (for 3:1 system) was then added to the resultant solution and stirred for 2 more hours. Then stoichiometric amount of deionised water (4.05 mL) was added using capillary addition pump over a period of 0.5 hours. This solution was kept under stirring overnight at room temperature. The pH of the slightly milky white solution was found to be >7. The resultant solution was placed in an autoclave, heated to 265 °C in 4 hours with a resultant pressure of 60-80 atm, kept for 10 min, vented to obtain an aerogel material and further dried at 120 °C to remove the traces of solvent. Example 4 Preparation of nanoternary Ni+Mg/AI ((0.9+2.1)/!) system In aerogel method, magnesium turnings (1.68g, 0.07M) were allowed to react with freshly dried methanol (70 mL) under argon flow. Under vigorous stirring, dry toluene (210 mL) was added to resultant magnesium methoxide solution and stirred for 2 hours. Aluminum isopropoxide (6.757 g, 0.033M) was then added to resultant solution and stirred for 2 more hours. Nickel acetylacetonate (7.76 g, 0.03 M) (for 3:1 system) was added to the resultant solution and stirred for 2 more hours. Then stoichiometric amount of deionised water (5.38 mL) was added using capillary addition pump over a period of 0.5 hours. This solution was kept under stirring overnight at room temperature. The pH of the slightly milky white solution was found to be >7. The resultant solution was placed in an autoclave, heated to 265 °C in 4 hours, kept for 10 minutes with a resultant pressure of 120-130 atm, vented to obtain an aerogel material and further dried at 120 °C to remove the traces of solvent. Example 5 The self-assembly of the nanobinary Mg2"1" and A13+ is done at room temperature by adding sodium carbonate (0.025 M/20 mL) to the nanoparticles (0.1 g) and stirred for 6 hours. The slurry was filtered, washed till the filtrate was neutral and o ven dried at 100 °C. Example 6 Self-assembly of nanobinary Mg2+ and A13+ is done at room temperature by adding disodium hydrogen orthophosphate (50 mL, 0.1 M) to the nanoparticles (0.5 g) and stirred for 6 hours. The slurry was filtered, washed till filtrate was neutral and o ven dried at 100 °C. Example 7 The self-assembly of nanobinary Mg2+ and A13+ is done at room temperature by adding potassium dichromate (35 mL, 0.1 M) to the nanoparticles (0.5 g) and stirred for 6 hours. The slurry was filtered, washed till the filtrate is colorless and oven dried at 100°C. Example 8 The self-assembly of nanobinary Mg2+ and A13+ is done at room temperature by dissolving 1.0 g of Ibuprofen in 55 mL of 0.1 M of sodium hydroxide solution to the solution nanoparticles (0.1 g) is added and stirred for 6 hours. The slurry was filtered, washed till the filtrate was neutral and oven dried at 100 °C. Example 9 The self-assembly of the nanoternary Ni2+-Mg2+ and A13+ is done at room temperature by adding sodium carbonate (0.025 M/20 mL) to the nanoparticles (0.1 g) and stirred for 6 hours. The slurry was filtered, washed till the filtrate was neutral and oven dried at 100 °C. The main advantages of the present invention are 1. A novel method for the preparation of homogeneous nanobinary and ternary metal oxy/ hydroxides. 2. The nano materials have high surface area. 3. The particle size of the materials is very low. 4. The nano oxy/ hydroxide material has potential applications as catalysts, adsorbents. 5. The self-assembly of the nano materials with anions leads to the formation of normal LDHs. 6. This self-assembly phenomena has potential applications as biomaterials for controlled drug delivery and gene reservoirs, preparation of thin films and membranes. We claim: 1. A process for the preparation of layered double hydroxides from homogeneous nandbinary or ternary metal oxy/hydroxide of LDH with high surface area and 1-10 nm particle size by an aerogel protocol, comprising i) hydrolysing a metal alkoxides or metal acetylacetonates in a solvent mixture selected from alcohols and hydrocarbons, by controlled addition of deionised water or a mixture thereof with alcohols, aging for 6 to 16 hours, ii) followed by hydrothermal treatment, iii) supercritical drying to obtain a free flow powder of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH, iv) adding anions selected from the group consisting of carbonates, phosphates, chromates, ibuprofen, salicylic acid and tartaric acid to self assemble the free flowing powder into normal layered double hydroxides. 2. A process as claimed in claim 1, wherein the metal in metal alkoxides/acetylacetonates is selected from the group consisting of bivalent metals ions comprising essentially of Mg2+, and trivalent metal ions consisting essentially of Al3+ 3. A process as claimed in claim 2, wherein the bivalent metal ions comprise Mg2+ and one or more bivalent metal ions selected from the group consisting of Ni2+ , Cu2+ , Co2+ , Zn2+ , Fe2+ and Mn2+ ions. 4. A process as claimed in claim 2, wherein the trivalent metal ions comprise Al+ and one or more trivalent metal ions selected from the group consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3+, V3+, Ti3+, La3+ and In3+ ions. 5. A process as claimed in claim 2, wherein the ratio of bivalent to trivalent metal ions is in the range of 1-5. 6. A process as claimed in claim 1, wherein the hydrothermal treatment is carried out at a temperature in the range of 100 to 300°C and pressure in the range of 50 to 150 atm. 7. A process as claimed in claim 1 wherein the hydrolysis comprises homogenization of metal precursors in hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric amount of deionised water. 8. A process as claimed in claim 1 wherein the metal alkoxides used are selected from the group consisting of methoxide, ethoxide, isomers of propoxide, butoxide and pentoxide. 9. A process as claimed in claim 5, wherein the ratio of bivalent to trivalent metal ions is preferably 2 to 3. 10. A process as claimed in claim 1, wherein the solvent mixture used is selected from a mixture of any of hexane, toluene, xylene, methanol, ethanol and butanol. 11. A process as claimed in claim 1, wherein the aging is preferably effected in a time period of 10 to 12 hours. 12. A process as claimed in claim 1, wherein the reaction mixture is hydrothermally heated at a temperature of 1°C per minute to a temperature in the range of 260 to 280°C, and kept for 5 to 10 minutes under higher pressures from 60 to 120 atm. 13. A process as claimed in claim 1, wherein the solvent mixture is vented out at super critical conditions to obtain a free flow of nano LDH. 14. A process as claimed in claim 1, wherein the recovered solvent free aerogel is dried overnight at 120ºC to remove the traces of solvent. 15. A process as claimed in claim 1, wherein the surface areas of homogeneous nanobinary and ternary materials range from 500-700 m2/g. 16. A process as claimed in claim 1, wherein the self assembled nanostructured LDH is obtained in the form of a hexagonal, fibrous, membrane or thin film. 17. A process for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH substantially as herein describe with reference to examples accompanying this specification.

Full Text

Field of the invention
The present invention relates to aprocess for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH.In particular it relates to a process for preparing and self-assembly of nanobinary and ternary metal oxy/hydroxides with high surface area and 1-10 nm size by aerogel procedure, involving homogenization of metal organic precursors in solvent mixture, controlled hydrolysis, gelation, hydrothermal treatment and finally supercritical drying of solvent.
During the self-assembly, the nano materials can be modulated into thin films, nano fibers, membranes, layered structures embedded with intercalated anions comprising of inorganic and organic anions selected from carbonates, phosphates, chromates, ibuprofen, dichlorofenec, salicylic acid, tartaric acid, dyes, and any other similar anions. These self- assembled materials find applications as catalysts, gene reservoirs, controlled drug release, solar energy harvesters. Background of the invention
Nano materials have generated unprecedented interest due to their unusual physical and chemical properties with wide and divergent applications in optics, electronics, magnetics, mechanics and catalysis. Nanocrystalline metal oxides exhibit unparalleled destructive adsorption properties of acid gases, polar organics, and even chemical/biological warfare agents. Due to high surface area, these nanostructured solid materials display good catalytic activity in isomerisation, alkylation, reforming and dehydrohalogenation reactions.
Generally, aerogel samples are prepared by supercritical drying of a gel from a sol-gel reaction. The aerogel has a specific high surface area with low density. Due to its physical characteristics, aerogel sample is useful as a catalyst or as a carrier for a catalyst.
LDHs, which consist of alternating cationic M111-X M"'X (0H)2X+ and anionic An-.zH20 layers have received much attention in recent times in view of their potential applications as catalysts, adsorbents, biomateriais for controlled drug delivery and gene reservoirs.
Reference is made to Nanostnictured Materials, 1999, 11, 1091 wherein nano particles of Zinc oxide and alumina were prepared independently by chemical arrested precipitation and then converted into nanocomposites by wet mixing. The inherent disadvantage of this protocol is the development of non-homogeneous material.

Reference is made to Journal of Solid State Chemistry, 2002, 165, 193
wherein binary oxides like titanium dioxide and tin oxide are prepared by stearic acid
method wherein particle size range from 10-15 nanometers. The drawback is the
system is non- homogeneous.
Reference is made to Chemistry of Materials, 2002, 14, 2922 wherein binary
alumina and magnesium oxides were prepared by sol-gel method. The ratios of the
alumina and magnesium oxides were not related to the normal hydrotalcites. The
drawback is the system is non- homogeneous.
Reference is made to Nature, 2000, 403, 65 wherein the homogeneous
nanobinary barium oxide and alumina were synthesized by reverse microemulsion
technique. The particle size ranges from 3-10 nanometers. The drawback is use of
expensive protocol.
Reference is made to Microporous and Mesoporous Materials, 2000, 39, 229
wherein the nano layered double hydroxides were prepared by sol-gel method. The
drawbacks are the size of the particles are high, ranging from 300-600 nanometers and
the surface area of the samples lower ranging from 240-270 m2/g.
Reference is made to Chemistry of Materials, 2002, 14, 4286 wherein nanolayered
double hydroxides with uniform crystal size were prepared by co-precipitation
in colloid mill and aging for 100°C for 13 h. The drawback is that the particle size
obtained in this method is about 60-80 nanometers.
Reference is made to Journal of American Chemical Society, 2000, 122, 3530
wherein the zeolite nanoparticles assembles into thin films, membranes, or fibers.
Reference is also made to Angewandte Chemie, 2002, 41, 1188 wherein the
quasi-spherical zinc oxide nanoparticles assemble into nanorods.
Objects of the invention
The main object of the present invention is to provide a process for preparing
homogeneous nanobinary and ternary metal oxy/hydoxides.
It is another object of the invention to provide a process for preparing nano
materials with high surface area and low particle size.
It is another object of the invention to provide a process for the preparation of
nano oxy/ hydroxide material with applications as catalysts and adsorbents.
Yet another object of the invention is to provide a process for preparing nanomaterials
by self-assembly with anions leading to the formation of normal LDHs with
applications as biomaterials for controlled drug delivery and gene reservoirs, preparation of thin films and membranes. Summary of the invention
The present invention provides a process for the synthesis of homogeneous nanobinary oxy/hydroxides composed of Mg2+ and Al3+, and nanoternary oxy/hydroxides comprising of Ni, Mg and Al by the aerogel protocol for the first time.
Accordingly, the present invention provides a process for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH with high surface area and 1-10 nm particle size by an aerogel protocol, comprising i) hydrolysing a metal alkoxides or metal acetylacetonates in a solvent mixture selected from alcohols and hydrocarbons, by controlled addition of deionised water or a mixture thereof with alcohols, aging for 6 to 16 hours, ii) followed by hydrothemnal treatment, iii) supercritical drying to obtain a free flow powder of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH, iv) adding anions selected from the group consisting of carbonates, phosphates, chromates, ibuprofen, salicylic acid and tartaric acid to self assemble the free flowing powder into normal layered double hydroxides.
In one embodiment of the invention, the metal in the metal alkoxides/acetylacetonates is selected from the group consisting of bivalent metals ions comprising essentially of Mg^"*^, and trivalent metal ions consisting essentially of
Al2+.
In another embodiment of the invention, the bivalent metal ions comprise Mg2+ and one or more bivalent metal ions selected from the group consisting of Ni2+, Cu2+,Co2+, Zn2+, Fe2+ and Mn2+ ions.
In yet another embodiment of the invention, the trivalent metal ions comprise AP+, and one or more trivalent metal ions selected from the group consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3+, V3+,Ti3+, La3+ and In3+ ions.
In a further embodiment of the invention, the ratio of bivalent to trivalent metal ions is in the range of from 1-5.
In another embodiment of the invention, the hydrothermal treatment is carried out at a temperature in the range of 100 to 300°C and pressure in the range of 50 to 150atm.
In an embodiment of the present invention, the hydrolysis comprises
homogenization of metal precursors in hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric amount of deionised water.

In an embodiment of the present invention, the metal alkoxides used are
selected from the group consisting of methoxide, ethoxide, isomers of propoxide,
butoxide and pentoxide.
In another embodiment of the present invention, the ratio of bivalent to
trivalent metal ions is 2 to 3.
In an embodiment of the present invention, the solvent mixture used is selected
from a mixture of any of hexane, toluene, xylene, methanol, ethanol and butanol.
In an embodiment of the present invention, the aging is preferably effected in
a time period of 10 to 12 hours.
In another embodiment of the present invention, the reaction mixture is
hydrothermally heated at a temperature of 1°C per minute to a temperature in the
range of 260 to 280°C, and kept for 5 to 10 minutes under higher pressures from 60 to
120atm.
In still another embodiment of present invention, the solvent mixture is vented
out at super critical conditions to obtain a free flow of nano LDH.
In yet another embodiment of the present invention, the recovered solvent free
aerogel is dried overnight about 120°C to remove the traces of solvent.
In yet another embodiment of the present invention, the surface areas of
homogeneous nanobinary and ternary materials range from 500-700 m2/g.
In yet another embodiment of the present invention, particle size of the
homogeneous nanobinary and ternary materials ranges from 1-10 nm.
In still another embodiment of the present invention, the nanoparticles selfassemble
on treatment with sodium carbonate/ phosphate/ chromate/ ibuprofen,
dicholorofenec solution at room temperature to normal layered double hydroxides.
In a further embodiment of the invention, the self assembled nanostructured
LDH is obtained in the form of a hexagonal, fibrous, membrane or thin film.
The present invention also provides a process for the preparation of selfassembled
layered double hydroxides made of homogeneous nanobinary or ternary
metal oxy/hydroxide of LDH of high surface area and 1-10 nm particle size,
comprising hydrolyzing a metal aikoxide or metal acetylacetonate in a solvent
mixture selected from alcohols and hydrocarbons, by controlled addition of deionised
water or a mixture thereof with alcohols, aging for 6 to 16 hours, followed by
hydrothermally treating and finally supercritical drying to obtain a free flow powder
of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH, adding anions
selected from the group consisting of carbonates, phosphates, chromates, ibuprofen,
salicylic acid and tartaric acid to self assemble the free flowing powder into normal
layered double hydroxides.
In one embodiment of the invention, the metal in the metal
alkoxides/acetylacetonates is selected from the group consisting of bivalent metals
ions comprising essentially of Nig2"1", and trivalent metal ions consisting essentially of
A13+.
In another embodiment of the invention, the bivalent metal ions comprise
Mg2* and one or more bivalent metal ions selected from the group consisting of Ni2+,
Cu2+, Co2+, Zn2+, Fe2+ and Mn2* ions.
In yet another embodiment of the invention, the trivalent metal ions comprise
AP+ and one or more trivalent metal ions selected from the group consisting of Ga3+,
Ni3+, Co3+, Fe3+, Mn3+, Cr3*, V3+, Ti3+, La3+ and In3* ions.
In a further embodiment of the invention, the ratio of bivalent to trivalent^
metal ions is in the range of from 1-5.
In another embodiment of the invention, the hydrothermal treatment is carried
out at a temperature in the range of 100 to 300°C and pressure in the range of 50 to
ISOatm.
In an embodiment of the present invention, the hydrolysis comprises
homogenization of metal precursors in hydrocarbon-alcohol solvent followed by
controlled addition of stoichiometric amount of deionised water.
In an embodiment of the present invention, the metal alkoxides used are
selected from the group consisting of methoxide, ethoxide, isomers of propoxide,
butoxide and pentoxide.
In another embodiment of the present invention, the ratio of bivalent to
trivalent metal ions is 2 to 3.
In an embodiment of the present invention, the solvent mixture used is selected
from a mixture of any of hexane, toluene, xylene, methanol, ethanol and butanol.
In an embodiment of the present invention, the aging is preferably effected in
a time period of 10 to 12 hours.
In another embodiment of the present invention, the reaction mixture is
hydrothermally heated at a temperature of 1 er minute to a temperature in the
range of 260 to 280°C, and kept for 5 to 10 minutes under higher pressures from 60 to
120atm.
In still another embodiment of present invention, the solvent mixture is vented
out at super critical conditions to obtain a free flow of nano LDH.
In yet another embodiment of the present invention, the recovered solvent free
aerogel is dried overnight about 120°C to remove the traces of solvent.
In yet another embodiment of the present invention, the surface areas of
homogeneous nanobinary and ternary materials range from 500-700 m2/g.
In yet another embodiment of the present invention, particle size of the
homogeneous nanobinary and ternary materials ranges from 1-10 nm.
In still another embodiment of the present invention, the nanoparticles selfassemble
on treatment with sodium carbonate/ phosphate/ chromate/ ibuprofen,
dicholorofenec solution at room temperature to normal layered double hydroxides.
In a further embodiment of the invention, the self assembled nanostructured
LDH is obtained in the form of a hexagonal, fibrous, membrane or thin film.
Detailed Description of the Invention
The novelty of the present invention relates to a process for preparing and selfassembly
of nanobinary and ternary metal oxy/hydroxides of Mg-Al binary (Mg/Al
ratios 2:1 and 3:1) and Ni-Mg-Al ternary systems [(Mg+Ni)/Al ratios (1.3+0.7): 1 and
(1.9+1.1): 1] by aerogel procedure, involving homogenization of metal organic
precursors in solvent mixture, controlled hydrolysis, gelation, hydrothermal treatment
and finally supercritical drying of solvent. The novelty of the present invention
provides a process for manufacturing of homogeneous nanobinary and ternary metal
oxy/hydroxides by aerogel method with an increased surface area. The self-assembly
of the nano metal oxy/ hydroxides when mediated by anion forms normal layered
double hydroxides. These self- assembled materials finds applications as catalysts,
gene reservoirs, controlled drug release, solar energy harvesters.
The nanobinary and ternary metal oxy/hydoxides have particle size ranging
from 1-10 nanometers and high surface area in the range of 500-700 m2/g. Preferred
compositions are made from alkoxides and acetylacetonates of the desired metals. The
nanobinary and ternary metal oxy/hydoxides prepared in the present invention have
an excellent self-assembling property and can be modulated into thin films, fibers,
membranes, when mediated by anions selected from inorganic and organic anions
such as carbonates, phosphates, chromates, ibuprofen, dichlorofenec, salicylic acid,
tartaric acid, dyes, and any other similar anions. The unprecedented self-assembly of
these nanoparticles driven by anion to normal LDH, helps in controlled drug release,
solar energy harvester, gene reservoir.
The process of the present invention generally comprises an aerogel protocol,
comprising hydrolysis of metal alkoxides /acetylacetonates selected from bivalent
metals ions comprising Mg2+ or any other metals consisting of Ni2+, Cu2+, Co2+, Zn2+,
Fe2+ and Mn2+ ions and trivalent metal ions selected from A13+ and optionally other
metals consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3^, V3+, Ti3+, La3+ and In3+ ions
in different ratios of M(II)/M(III) ranging from 1-5 in a solvent mixture selected from
alcohols /hydrocarbons, by controlled addition of deionised water/their mixtures with
alcohols, aging for 6 to 16 hours, followed hydrothermal treatment at temperatures
ranging from 100 to 300 °C and pressures ranging from 50 to 150 atm and finally
supercritical drying to obtain a free flow powder and the nanostructured LDH self
assembled by the addition of anions selected from carbonates, phosphates, chromates,
ibuprofen, salicylic acid, tartaric acid, etc, into normal layered double hydroxides in
hexagonal, fibrous, membrane or thin film.
Hydrolysis preferably involves homogenization of metal precursors in
hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric
amount of deionised water. Metal alkoxides used are selected from methoxide,
ethoxide, isomers of propoxide, butoxide and pentoxide. Preferred ratio of bivalent
and trivalent metal ions is 2 to 3.
The solvent mixture used is selected from hexane, toluene, xylene, methanol,
ethanol, butanol etc., and aging is preferably done for 10 to 12 hours. The reaction
mixture is hydrothermally heated with the ramping of temperature 1 °C per minute to
260 to 280 °C, and kept for 5 to 10 minutes under higher pressures from 60 to 120 atm.
The solvent mixture is vented out at super critical conditions to obtain a free flow of
nano LDH. The recovered solvent free aerogel is dried overnight about 120 °C to
remove the traces of solvent. The surface areas of homogeneous nanobinary and
ternary materials range from 500-700 m2/g and particle size ranges from 1-10 nm. It is
observed that the nanoparticles self-assemble on treatment with sodium carbonate/
phosphate/ chromate/ ibuprofen, dicholorofenec solution at room temperature to
normal layered double hydroxides.
The following examples are given by way of illustration of the present
invention and therefore should not be constructed to limit the scope of invention.
Example 1
Preparation of nanobinary Mg/Al (2/1) system
In aerogel method, magnesium turnings (2.4g, 0.1M) were allowed to react
with freshly dried methanol (100 mL) under argon flow by stirring. Dry toluene (300
mL) was added to the resultant magnesium methoxide solution and continued stirring
for2 hours. Aluminum isopropoxide (10.235 g, 0.05M) (for 2:1 system) was then
added to the resultant solution and stirred for 2 more hours. Then stoichiometric
amount of deionised water (4.85 mL) was added using capillary addition pump over a
period of 0.5 h. This solution was kept under stirring overnight at room temperature.
The pH of the slightly milky white solution was found to be >7. The resultant solution
was placed in an autoclave, heated in 4 hours to 265 °C with a resultant pressure of
60-80 atm, kept for 10 min, vented to obtain an aerogel material and further dried at
120 °C to remove the traces of solvent.
Example 2
Preparation of nanoternary Ni+Mg/Al ((0.7+1.3)/!) system
In aerogel method, magnesium turnings (1.56 g, 0.13M) were allowed to react
with freshly dried methanol (65 mL) under argon flow. Under vigorous stirring, dry
toluene (195 mL) was added to the resultant magnesium methoxide solution and
stirred for 2 hours. Aluminum isopropoxide (20.475 g, 0.1M) was then added to the
resultant solution and stirred for 2 more hours. Nickel acetylacetonate (17.99 g, 0.07
M) (for 2:1 system) was added to the resultant solution and stirred for 2 more hours.
Then stoichiometric amount of deionised water (10.26 mL) was added using capillary
addition pump over a period of 0.5 hours. This solution was kept under stirring
overnight at room temperature. The pH of the slightly milky white solution was found
to be >7. The resultant solution was placed in an autoclave, heated to 265 °C in 4
hours with a resultant pressure of 120-130 atm, kept for 10 minutes, vented to obtain
an aerogel material and further dried at 120 °C to remove the traces of solvent.
Example 3
Preparation of nanobinary Mg/Al (3/1) system
In aerogel method, magnesium turnings (1.8 g, 0.075 M) were allowed to react
with freshly dried methanol (75 mL) under argon flow. Under vigorous stirring, dry
toluene (225 mL) was added to the resultant magnesium methoxide solution and
stirred for 2 hours. Aluminum isopropoxide (5.12 g, 0.025M) (for 3:1 system) was
then added to the resultant solution and stirred for 2 more hours. Then stoichiometric
amount of deionised water (4.05 mL) was added using capillary addition pump over a
period of 0.5 hours. This solution was kept under stirring overnight at room
temperature. The pH of the slightly milky white solution was found to be >7. The
resultant solution was placed in an autoclave, heated to 265 °C in 4 hours with a
resultant pressure of 60-80 atm, kept for 10 min, vented to obtain an aerogel material
and further dried at 120 °C to remove the traces of solvent.
Example 4
Preparation of nanoternary Ni+Mg/AI ((0.9+2.1)/!) system
In aerogel method, magnesium turnings (1.68g, 0.07M) were allowed to react
with freshly dried methanol (70 mL) under argon flow. Under vigorous stirring, dry
toluene (210 mL) was added to resultant magnesium methoxide solution and stirred
for 2 hours. Aluminum isopropoxide (6.757 g, 0.033M) was then added to resultant
solution and stirred for 2 more hours. Nickel acetylacetonate (7.76 g, 0.03 M) (for 3:1
system) was added to the resultant solution and stirred for 2 more hours. Then
stoichiometric amount of deionised water (5.38 mL) was added using capillary
addition pump over a period of 0.5 hours. This solution was kept under stirring
overnight at room temperature. The pH of the slightly milky white solution was found
to be >7. The resultant solution was placed in an autoclave, heated to 265 °C in 4
hours, kept for 10 minutes with a resultant pressure of 120-130 atm, vented to obtain
an aerogel material and further dried at 120 °C to remove the traces of solvent.
Example 5
The self-assembly of the nanobinary Mg2"1" and A13+ is done at room
temperature by adding sodium carbonate (0.025 M/20 mL) to the nanoparticles (0.1 g)
and stirred for 6 hours. The slurry was filtered, washed till the filtrate was neutral and
o ven dried at 100 °C.
Example 6
Self-assembly of nanobinary Mg2+ and A13+ is done at room temperature by
adding disodium hydrogen orthophosphate (50 mL, 0.1 M) to the nanoparticles (0.5 g)
and stirred for 6 hours. The slurry was filtered, washed till filtrate was neutral and
o ven dried at 100 °C.
Example 7
The self-assembly of nanobinary Mg2+ and A13+ is done at room temperature
by adding potassium dichromate (35 mL, 0.1 M) to the nanoparticles (0.5 g) and
stirred for 6 hours. The slurry was filtered, washed till the filtrate is colorless and
oven dried at 100°C.
Example 8
The self-assembly of nanobinary Mg2+ and A13+ is done at room temperature
by dissolving 1.0 g of Ibuprofen in 55 mL of 0.1 M of sodium hydroxide solution to
the solution nanoparticles (0.1 g) is added and stirred for 6 hours. The slurry was
filtered, washed till the filtrate was neutral and oven dried at 100 °C.
Example 9
The self-assembly of the nanoternary Ni2+-Mg2+ and A13+ is done at room
temperature by adding sodium carbonate (0.025 M/20 mL) to the nanoparticles (0.1 g)
and stirred for 6 hours. The slurry was filtered, washed till the filtrate was neutral and
oven dried at 100 °C.
The main advantages of the present invention are
1. A novel method for the preparation of homogeneous nanobinary and ternary
metal oxy/ hydroxides.
2. The nano materials have high surface area.
3. The particle size of the materials is very low.
4. The nano oxy/ hydroxide material has potential applications as catalysts,
adsorbents.
5. The self-assembly of the nano materials with anions leads to the formation of
normal LDHs.
6. This self-assembly phenomena has potential applications as biomaterials for
controlled drug delivery and gene reservoirs, preparation of thin films and
membranes.

We claim:
1. A process for the preparation of layered double hydroxides from homogeneous nandbinary or ternary metal oxy/hydroxide of LDH with high surface area and 1-10 nm particle size by an aerogel protocol, comprising i) hydrolysing a metal alkoxides or metal acetylacetonates in a solvent mixture selected from alcohols and hydrocarbons, by controlled addition of deionised water or a mixture thereof with alcohols, aging for 6 to 16 hours, ii) followed by hydrothermal treatment, iii) supercritical drying to obtain a free flow powder of homogeneous nanobinary or ternary metal oxy/hydroxide of LDH, iv) adding anions selected from the group consisting of carbonates, phosphates, chromates, ibuprofen, salicylic acid and tartaric acid to self assemble the free flowing powder into normal layered double hydroxides.
2. A process as claimed in claim 1, wherein the metal in metal alkoxides/acetylacetonates is selected from the group consisting of bivalent metals ions comprising essentially of Mg2+, and trivalent metal ions consisting essentially of Al3+
3. A process as claimed in claim 2, wherein the bivalent metal ions comprise Mg2+ and one or more bivalent metal ions selected from the group consisting of Ni2+ , Cu2+ , Co2+ , Zn2+ , Fe2+ and Mn2+ ions.
4. A process as claimed in claim 2, wherein the trivalent metal ions comprise Al+ and one or more trivalent metal ions selected from the group consisting of Ga3+, Ni3+, Co3+, Fe3+, Mn3+, Cr3+, V3+, Ti3+, La3+ and In3+ ions.
5. A process as claimed in claim 2, wherein the ratio of bivalent to trivalent metal ions is in the range of 1-5.
6. A process as claimed in claim 1, wherein the hydrothermal treatment is carried out at a temperature in the range of 100 to 300°C and pressure in the range of 50 to 150 atm.
7. A process as claimed in claim 1 wherein the hydrolysis comprises homogenization of metal precursors in hydrocarbon-alcohol solvent followed by controlled addition of stoichiometric amount of deionised water.
8. A process as claimed in claim 1 wherein the metal alkoxides used are selected from the group consisting of methoxide, ethoxide, isomers of propoxide, butoxide and pentoxide.

9. A process as claimed in claim 5, wherein the ratio of bivalent to trivalent metal ions is preferably 2 to 3.
10. A process as claimed in claim 1, wherein the solvent mixture used is selected from a mixture of any of hexane, toluene, xylene, methanol, ethanol and butanol.
11. A process as claimed in claim 1, wherein the aging is preferably effected in a time period of 10 to 12 hours.
12. A process as claimed in claim 1, wherein the reaction mixture is hydrothermally heated at a temperature of 1°C per minute to a temperature in the range of 260 to 280°C, and kept for 5 to 10 minutes under higher pressures from 60 to 120 atm.
13. A process as claimed in claim 1, wherein the solvent mixture is vented out at super critical conditions to obtain a free flow of nano LDH.
14. A process as claimed in claim 1, wherein the recovered solvent free aerogel is dried overnight at 120ºC to remove the traces of solvent.
15. A process as claimed in claim 1, wherein the surface areas of homogeneous
nanobinary and ternary materials range from 500-700 m2/g.
16. A process as claimed in claim 1, wherein the self assembled nanostructured LDH is obtained in the form of a hexagonal, fibrous, membrane or thin film.
17. A process for the preparation of layered double hydroxides from homogeneous nanobinary or ternary metal oxy/hydroxide of LDH substantially as herein describe with reference to examples accompanying this specification.

Documents:

499-DEL-2003-Abstract-(10-10-2008).pdf

499-del-2003-abstract.pdf

499-DEL-2003-Claims-(10-10-2008).pdf

499-del-2003-claims.pdf

499-DEL-2003-Correspondence-Others-(10-10-2008).pdf

499-del-2003-correspondence-others.pdf

499-del-2003-correspondence-po.pdf

499-DEL-2003-Description (Complete)-(10-10-2008).pdf

499-del-2003-description (complete).pdf

499-DEL-2003-Form-1-(10-10-2008).pdf

499-del-2003-form-1.pdf

499-del-2003-form-18.pdf

499-DEL-2003-Form-2-(10-10-2008).pdf

499-del-2003-form-2.pdf

499-DEL-2003-Form-3-(10-10-2008).pdf

499-del-2003-form-3.pdf

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Patent Number

225697

Indian Patent Application Number

499/DEL/2003

PG Journal Number

13/2009

Publication Date

27-Mar-2009

Grant Date

20-Nov-2008

Date of Filing

27-Mar-2003

Name of Patentee

COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH

Applicant Address

RAFI MARG, NEW DELHI-110 001,INDIA

Inventors:

#	Inventor's Name	Inventor's Address
1	BOYAPATI MANORANJAN CHOUDARY	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA
2	VALLABHA SWARNA JAYA	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA
3	BONTHA RAMACHANDRA REDDY	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA
4	MANNEPALLI LAKSHMI KANTAM	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA
5	MANDAPATI MOHAN RAO	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA
6	KOTTAPALLI KOTESWARA RAO	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA
7	KONDAPURAM VIJAYA RAGHAVAN	CHEMICAL TECHNOLOGY, HYDERABAD-500 007, ANDHRA PRADESH,INDIA

PCT International Classification Number

B32B 1/00

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1			NA