Patent Grant
10930406
The present disclosure relates to the technical field of radioactive waste disposal, in particular to a method of oxidative digestion of a radioactively contaminated carbonaceous material (carbonaceous material) in liquid phase.
A great amount of radioactively contaminated carbonaceous materials are produced during nuclear-related processes, for example, graphitic layers in nuclear reactors for moderating/reflecting neutrons, graphite crucibles and graphite molds used in smelting, casting and analyzing radioactive materials, resin used in the disposal of radioactive waste liquid and so forth. For the disposal of radioactively contaminated carbon materials, there is no thorough and mature solution so far. Existing incineration technology can barely be used for volume reduction of a carbonaceous material with a low level of radioactive contamination. However, once a carbonaceous material with a relatively high level of radioactive contamination is involved, e.g. graphite crucibles and graphite molds contaminated by uranium, the incineration of such radioactively contaminated carbonaceous materials is infeasible due to the fact that the current incinerator cannot ensure that the uranium aerosol is thoroughly cut off.
Carbon, especially high-purity carbon used in the nuclear industry, is an excellent heat conductor, and this property renders carbon unable to store heat, and if carbon is to be oxidized through incineration, persistent high energy input is required to maintain the temperature of carbon above 1000° C., this process is of high energy consumption and the deterioration of the sealing performance of the device at a high temperature would be accompanied by the risk of radioactive aerosol leakage. Steam reforming utilizes high-temperature steam to oxidize carbon into a gas (C+H2O→CO+CO+H2), which may also be a disposal mode for radioactively contaminated carbonaceous materials. However, the significant oxidation of carbon by water occurs at a temperature above 1000° C., while it is highly likely for matching failure to occur to a connecting piece of the device under such condition due to thermal expansion, hereby resulting in a radioactive aerosol leakage.
Accordingly, as for the volume-reduction and weight-reduction disposal of radioactively contaminated carbonaceous materials, it is necessary to moderate the reaction conditions as much as possible, to inhibit the generation of radioactive aerosol, and to ensure a safe, stable and reliable disposal process.
An object of the present disclosure is to provide a technical solution for a method of oxidative digestion of a radioactively contaminated carbonaceous material in liquid phase, in the light of the deficiencies existing in the prior art, wherein the technical solution utilizes thermal treatment to make carbon enter the space between molybdenum atoms, which reduces the particle size of carbon and enhances the chemical reactivity of carbon. Consequently, carbon in the space between molybdenum atoms is oxidized in liquid phase into a gas by an oxidant, and simultaneously, the molybdenum-containing moiety is converted into a water-soluble substance, hereby achieving effects of mild reaction conditions, low energy consumption, high operational safety and conduciveness to recovery of elements attached to the carbonaceous material.
The present solution is realized through the following technical measures:
A method of oxidative digestion of a radioactively contaminated carbonaceous material in liquid phase, comprising the following steps:
a. milling a mixture of a molybdenum-containing substance and a carbonaceous material by using a planetary ball mill with a fixed ball mill revolution speed, to provide first-stage powders;
b. placing the first-stage powders obtained in Step a) into a heating furnace, thermally treating the first-stage powders under a flowing gas, and then naturally cooling the first-stage powders to provide second-stage powders; and
c. adding the second-stage powders to water, and adding an oxidant, such that carbon contained therein is oxidized into a gas, and the molybdenum-containing moiety is converted into a water-soluble substance.
Preferably in the present solution: the component ratio between the carbonaceous material and the molybdenum-containing substance in Step a) is, in parts by weight, 1 part of the carbonaceous material to 2-50 parts of the molybdenum-containing substance.
Preferably in the present solution: the component ratio between the carbonaceous material and the molybdenum-containing substance in Step a) is, in parts by weight, 1 part of the carbonaceous material to 3.5-50 parts of the molybdenum-containing substance.
Preferably in the present solution: the component ratio between the carbonaceous material and the molybdenum-containing substance in Step a) is, in parts by weight, 1 part of the carbonaceous material to 2 parts, 3 parts, 3.5 parts, 10 parts, 15 parts, 20 parts, 30 parts, 40 parts or 50 parts of the molybdenum-containing substance.
Preferably in the present solution: the gas in Step b) is an inert gas or a gas mixture of hydrogen and an inert gas.
Preferably in the present solution: the oxidant in Step c) is one from ozone, hydrogen peroxide, permanganates, dichromates, or a free combination thereof.
Preferably in the present solution: the molybdenum-containing substance is one from molybdenum trioxide, molybdenum dioxide, hexaammonium molybdate, phosphomolybdic acid, silicomolybdic acid, and metallic molybdenum, or a free combination thereof.
Preferably in the present solution: the carbonaceous material is activated carbon or carbon nanotubes or graphite or carbon fibers or carbon black or resin.
Preferably in the present solution: the inert gas is argon, helium or nitrogen.
Preferably in the present solution: the thermal treatment in Step b) is realized at a temperature rise rate of 0.5-20° C./min, till a temperature of 500-1100° C., with the temperature being maintained for 1-6 hours.
Preferably in the present solution: the thermal treatment in Step b) is realized at a temperature rise rate of 0.5-20° C./min, till a temperature of 900-1100° C., with the temperature being maintained for 1-6 hours.
Preferably in the present solution: the thermal treatment in Step b) is realized at a temperature rise rate of 0.5° C./min, 1° C./min, 2° C./min, 5° C./min, 10° C./min or 20° C./min.
Preferably in the present solution: the heating in Step b) is performed till a temperature of 500° C., 600° C., 700° C., 750° C., 800° C., 900° C., 1000° C. or 1100° C.
Preferably in the present solution: the duration of temperature maintenance of the high temperature condition during the thermal treatment in Step b) is 1 hour, 2 hours, 4 hours, 5 hours or 6 hours.
The beneficial effects of the present solution can be determined from the preceding statement of the solution, the technical solution utilizes thermal treatment to make carbon enter the space between molybdenum atoms, which reduces the particle size of carbon and enhances the chemical reactivity of carbon. Consequently, carbon in the space between molybdenum atoms can be oxidized in liquid phase into a gas by an oxidant, and simultaneously, the molybdenum-containing moiety is converted into a water-soluble substance, hereby achieving effects of mild reaction conditions, low energy consumption, high operational safety and conduciveness to recovery of elements attached to the carbonaceous material.
Accordingly, compared with the prior art, the present disclosure has a substantive feature and represents a progress, and the beneficial effects of its implementation are also apparent.
Except for mutually exclusive features and/or steps, all the features or all the steps in the method or the process disclosed in the present specification may be combined with each other in any manner.
Unless expressly stated otherwise, any feature disclosed in the specification (including any appended claims, the abstract or the drawings) can be replaced by any other alternative feature that is equivalent or has a similar object. That is to say, unless expressly stated otherwise, each feature is only one example of a series of equivalent or similar features.
A method of oxidative digestion of a radioactively contaminated carbonaceous material in liquid phase, comprising the following steps:
(1) milling a mixture of a molybdenum-containing substance and a carbonaceous material by using a planetary ball mill at a fixed ball mill revolution speed, to provide first-stage powders;
(2) placing the first-stage powders obtained in Step (1) into a heating furnace, performing thermal treatment to the first-stage powders under a flowing gas, and then naturally cooling the same to provide second-stage powders;
(3) adding the second-stage powders to water, and adding an oxidant, such that carbon contained therein is oxidized into a gas, and molybdenum-containing moiety is converted into a water-soluble substance.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:20, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:20, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Activated carbon and molybdenum trioxide were mixed in a weight ratio of 1:15, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 700° C. at a temperature rise rate of 5° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 2 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % potassium permanganate water solution, and the digestion rate of the activated carbon was determined as 60% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and hexaammonium molybdate were mixed in a weight ratio of 1:40, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:30, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 600° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 48% after 1 hour.
(1) Graphite and phosphomolybdic acid were mixed in a weight ratio of 1:30, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and molybdenum dioxide were mixed in a weight ratio of 1:20, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and silicomolybdic acid were mixed in a weight ratio of 1:50, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 20° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 1 hour, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:5, and then placed in a ball mill pot and milled for 1 hour by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 500° C. at a temperature rise rate of 1° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 22% after 1 hour.
(1) D152 macroporous weak acid cation exchange resin and molybdenum trioxide were mixed in a weight ratio of 1:30, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 1000° C. at a temperature rise rate of 2° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the D152 macroporous weak acid cation exchange resin was determined as 100% after 1 hour.
(1) 717-type strong base anion exchange resin and molybdenum trioxide were mixed in a weight ratio of 1:30, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 1000° C. at a temperature rise rate of 2° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the 717-type strong base anion exchange resin was determined as 100% after 1 hour.
(1) Graphite and phosphomolybdic acid were mixed in a weight ratio of 1:40, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 0.5° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Natural flake graphite and metallic molybdenum were mixed in a weight ratio of 1:20, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 1100° C. at a temperature rise rate of 1° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:5, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in argon with a flowing rate of 100 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 200 ml of water acidized by nitric acid, and after blowing ozone therein at a velocity of 10 g/h for 5 hours, the digestion rate of the graphite was determined as 98%.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:4, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 5 ml/min and the hydrogen having a flowing rate of 95 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 0.5 hour.
(1) Activated carbon and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 700° C. at a temperature rise rate of 5° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 100 ml of 30 wt % potassium permanganate water solution, and the digestion rate of the activated carbon was determined as 40% after 1 hour.
(1) D152 macroporous weak acid cation exchange resin and molybdenum trioxide were mixed in a weight ratio of 1:6, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 1100° C. at a temperature rise rate of 0.5° C./min in argon with a flowing rate of 100 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 200 ml of water alkalized by sodium hydroxide, and after blowing ozone therein at a velocity of 10 g/h for 5 hours, the digestion rate of the resin was determined as 98%.
(1) Graphite and hexaammonium molybdate were mixed in a weight ratio of 1:50, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 1000° C. at a temperature rise rate of 5° C./min in argon with a flowing rate of 100 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 96% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:2, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 20° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 1 hour, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 62% after 1 hour.
(1) Graphite and phosphomolybdic acid were mixed in a weight ratio of 1:30, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 5° C./min in a nitrogen-hydrogen mixture with the nitrogen having a flowing rate of 5 ml/min and the hydrogen having a flowing rate of 95 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 90% after 1 hour.
(1) Graphite and molybdenum dioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in nitrogen with a flowing rate of 100 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 200 ml of water acidized by nitric acid, and after blowing ozone therein at a velocity of 10 g/h for 5 hours, the digestion rate of the graphite was determined as 85%.
(1) Graphite and silicomolybdic acid were mixed in a weight ratio of 1:50, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 700° C. at a temperature rise rate of 20° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 39% after 1 hour.
(1) 717-type strong base anion exchange resin and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 2° C./min in a helium-hydrogen mixture with the helium having a flowing rate of 5 ml/min and the hydrogen having a flowing rate of 95 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the 717-type strong base anion exchange resin was determined as 100% after 1 hour.
(1) Natural flake graphite and metallic molybdenum were mixed in a weight ratio of 1:50, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 1° C./min in helium with a flowing rate of 100 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 78% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:3.5, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 20° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 1 hour, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and silicomolybdic acid were mixed in a weight ratio of 1:50, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 900° C. at a temperature rise rate of 20° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 100% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:1.5, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 600° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 11% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 400° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 5% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 600° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 30 minutes, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 18% after 1 hour.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 600° C. at a temperature rise rate of 25° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 200 ml of water alkalized by sodium hydroxide, and after blowing ozone therein at a velocity of 10 g/h for 5 hours, the digestion rate of the graphite was determined as 16%.
(1) Graphite and palladium oxide were mixed in a weight ratio of 1:1, and then placed in a ball mill pot and milled for 5 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 600° C. at a temperature rise rate of 2° C./min in an argon-hydrogen mixture with the argon having a flowing rate of 30 ml/min and the hydrogen having a flowing rate of 50 ml/min, wherein the temperature was maintained for 5 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the loss rate of the graphite was determined after 1 hour as 53%.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:1, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 500° C. at a temperature rise rate of 2° C./min in argon with a flowing rate of 100 ml/min, wherein the temperature was maintained for 6 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 200 ml of water acidized by nitric acid, and after blowing ozone therein at a velocity of 10 g/h for 5 hours, the digestion rate of the graphite was determined as 10%.
(1) Graphite and molybdenum trioxide were mixed in a weight ratio of 1:10, and then placed in a ball mill pot and milled for 3 hours by using a planetary ball mill at a revolution speed of 300 r/min;
(2) 2 g of the obtained powders was placed in a tube furnace and heated to 400° C. at a temperature rise rate of 2° C./min in argon with a flowing rate of 100 ml/min, wherein the temperature was maintained for 4 hours, then the gas was turned off, and powders were obtained after natural cooling; and
(3) 1 g of the obtained powders was added to 20 ml of 30 wt % hydrogen peroxide, and the digestion rate of the graphite was determined as 8% after 1 hour.
Compared with the above comparative examples conducted under non-preferred conditions, it can be determined that the digestion rate of carbon materials is significantly improved and the treatment efficiency is significantly increased, when the amount of a molybdenum oxide group-containing substances, the ball mill revolution speed of the planetary ball mill, the milling duration of the planetary ball mill, the temperature maintained under the high temperature condition during the thermal treatment and the duration of temperature maintenance under the high temperature condition during the thermal treatment fall within the preferred condition ranges according to the present disclosure, hereby achieving the technical effects of mild reaction conditions, low energy consumption, high operational safety and conduciveness to recovery of elements attached to the carbonaceous material.
The present disclosure is not limited to the foregoing detailed description of the embodiments. The present disclosure extends to any novel feature disclosed in this specification or any novel combination thereof, as well as any step in a novel method or process disclosed or any novel combination thereof.
The present disclosure discloses a method of oxidative digestion of a radioactively contaminated carbonaceous material in liquid phase, wherein the method achieves mild reaction conditions, low energy consumption, and high operational safety, and significantly improves the efficiency of the digestive disposal of a carbonaceous material, which is conducive to recovery of elements attached to the carbonaceous material.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201610339632.X | May 2016 | CN | national |
The present disclosure is a continuation-in-part application of the international patent application No. PCT/CN2017/082560 filed on Apr. 28, 2017, which claims priority to Chinese patent application No. 201610339632.X filed on May 23, 2016. The contents of the above applications are hereby incorporated by reference.
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| Number | Date | Country | |
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| 20190096537 A1 | Mar 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2017/082560 | Apr 2017 | US |
| Child | 16198905 | US |
