US2018322975A1PendingUtilityA1
Method of making a mercury based compound, mercury based compound, methods of using the mercury based compound and uses of the mercury based compound
Est. expiryMay 12, 2035(~8.8 yrs left)· nominal 20-yr term from priority
Inventors:Suneel Navnitdas Parekh
C01P 2002/72C01G 13/04C01P 2002/86G21F 9/28G21F 5/00C01P 2004/61C01P 2002/89C01P 2004/04C01P 2002/74C01G 35/006C01P 2004/64G21F 9/06C01P 2002/82C01P 2006/42G21F 9/30C01G 13/006C01B 32/907G21G 5/00C01P 2004/03C01G 13/00G21B 3/00C01G 55/002G21Y 2002/60G21Y 2004/10C01G 53/006Y02E30/30C01G 53/82Y02E30/10
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Claims
Abstract
The present invention relates to a method of making a mercury based compound, to a mercury based compound and to methods of using the mercury based compound and to uses of the mercury based compound.
Claims
exact text as granted — not AI-modified1 . A method of fabricating a mercury based compound, the method comprising the steps of:
providing a pure mineral acid in a container; adding liquid mercury to the container; reacting the mercury and the mineral acid to form a mixture; and drying the mixture to form the mercury based compound in powder form.
2 . The method according to claim 1 ,
wherein the mineral acid is formed in the container before, after or during the step of adding the liquid mercury.
3 . The method according to claim 1 , wherein the mineral acid comprises at least one acid selected from the group of acids consisting of aqua regia, HNO 3 , HCl, H 2 SO 4 .
4 . The method according to claim 1 , wherein the ratio of mineral acid to liquid mercury is selected from the range of between at least substantially 0.1 to 1 and 10:1 of mineral acid to.
5 . The method according to claim 1 , wherein the step of drying is carried out at a temperature selected in the range of 80° to 150° C. for a time selected in the range of 30 minutes to 10 hours.
6 . The method according to claim 1 , further comprising the step of adding a solvent, with the solvent is selected from the group of solvents consisting of a polar solvent, formic acid, ethanol, acetone, ammonia, acetic acid, a non-polar solvent, toluene, benzene and combinations thereof.
7 . The method according to claim 1 , the method further comprising the step of:
separating residual liquid from the mixture prior to drying the mixture.
8 . The method according to claim 1 , further comprising at least one of the following steps:
maintaining an initial temperature of the mixture at room temperature; heating the mixture, e.g. up to a temperature at which the mineral acid is evaporated to dry the mercury based compound; and isolating compounds that do not contain liquid mercury from the mixture.
9 . The method according to claim 1 , wherein the step of adding the liquid mercury to the container takes place before the mineral acid is added to the container.
10 . A mercury based compound in powder form having the general chemical formula:
M 1 a X b where M 1 is selected from the group of compounds consisting of Hg, M x c M y d and a combination thereof, with M x being Hg and M y being an arbitrary element; where X is one of a halide, sulphate nitrate and a combination thereof; and where a, b, c and d are numbers selected between 0.1 and 10.
11 . The mercury based compound according to claim 10 , wherein the mercury based compound is obtained by:
providing a pure mineral acid in a container; adding liquid mercury to the container; reacting the mercury and the mineral acid to form a mixture; and drying the mixture to form the mercury based compound in powder form
12 . The mercury based compound according to claim 10 , wherein X is a halide and the halide is selected from the group of members consisting of chloride, bromide, fluoride and iodide.
13 . The mercury based compound according to claim 10 , wherein the mercury based compound is present in powder form at room temperature.
14 . The mercury based compound according to claim 13 , wherein particles of the powder have a minimum average dimension of width of at least 50 nm and a maximum average dimension of width of at most 20 μm.
15 . The mercury based compound according to claim 10 , wherein an XRD spectrum of the mercury based compound includes peaks corresponding to Di-mercury sulphate (Hg2O4 S1) and Calomel (Cl2Hg2), and wherein: the peaks present in the XRD spectrum show mercury based compounds that include at least one of C, N, O, Cl, and S; or the mercury based compound is paramagnetic.
16 . A method of producing metal compounds and metal elements in an endothermic reaction, the method comprising the steps of:
providing a metal target material, in the molten state, with the metal target material having a proton number of greater than or equal to 26, and adding a mercury based compound; wherein the mercury based compound reacts with the metal target material to transmutate elements; and wherein the mercury based compound has the general chemical formula: M 1 a X b , wherein M 1 is selected from the group of compounds consisting of Hg, M x c M y d and a combination thereof, with M x being Hg and M y being an arbitrary element; wherein X is one of a halide, sulphate nitrate and a combination thereof; and where a, b, c and d are numbers selected between 0.1 and 10.
17 . The method according to claim 16 , wherein the metal target material includes between 10 g and 1000000 Kg of, molten, metal target material.
18 . The method according to claim 16 , wherein a range of between 1 mg to 100 kg of the mercury based compound are added to the metal target material.
19 . The method according to claim 16 , wherein the ratio of mass between the mercury based compound and the metal target material is selected from the range 1:100000 to 1:100.
20 . The method according to claim 16 , wherein the mercury based compound comprises energy reacting with nuclei of the metal target material in order to create elements having at least one of a higher proton number and a higher neutron number.
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