Permeable reactive barrier composite material, and preparation method and applications thereof
A permeable reactive wall and composite material technology, applied in the field of permeable reactive wall composite materials and its preparation, can solve the problems of easily damaged reaction medium, cumbersome installation, and long time consumption, so as to achieve good structural stability, reduce production costs, The effect of improving structural stability
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[0026] The preparation method of the permeable reactive wall composite material of the present invention comprises the following steps (in the following steps, the amounts of components are all in parts by mass):
[0027] Step 1, weighing 1 to 2 parts of ferric nitrate, and preparing ferric nitrate solution;
[0028] Step 2, adding 10 parts of semi-coke powder to the ferric nitrate solution in step 1, and adding 1 part of ethanol for dispersion to make a mixed solution A;
[0029] In step 3, the mixed solution A in step 2 is sequentially subjected to ultrasonic impregnation, constant temperature oscillation, drying and grinding to make a mixture powder A of ferric nitrate-blue carbon powder;
[0030] Step 4, adding 1 to 4 parts of coal liquefaction residue to the mixture powder A in step 3, and mixing evenly to prepare mixture powder B;
[0031] Step 5, compressing the mixture powder B in step 4 into a cylinder;
[0032] In step 6, the cylinder in step 5 is placed in a tube ...
Embodiment 1
[0035] First crush the semi-coke powder and coal liquefaction residue to 200 mesh for later use. Weigh 1 part of ferric nitrate and prepare ferric nitrate solution; add 10 parts of 200-mesh blue charcoal powder into the ferric nitrate solution, and add 1 part of ethanol to disperse at the same time to prepare mixed solution A. After the mixture A was ultrasonicated for 4 hours, it was placed in a constant temperature oscillator at 40°C, shaken for 1 hour, and then dried in an oven at 105°C for 12 hours, and the dried black powder was ground to 200 mesh to obtain the mixture powder A. 2 parts of 200-mesh coal liquefaction residue and mixture powder A were fully mixed to prepare mixture powder B. The mixture powder B was cold-pressed into a cylinder with a diameter of 7 mm and a height of 10 mm under a pressure of 5 MPa, and a mass of 0.6 g. Put the cylinder in the tube furnace, set the heating rate at 20°C / s, the final temperature of physical activation at 900°C, the constant ...
Embodiment 2
[0037] First crush the semi-coke powder and coal liquefaction residue to 200 mesh for later use. Weigh 2 parts of ferric nitrate and prepare ferric nitrate solution; add 10 parts of 200-mesh blue charcoal powder into the ferric nitrate solution, and add 1 part of ethanol to disperse at the same time to prepare mixed solution A. After the mixture A was ultrasonicated for 4 hours, it was placed in a constant temperature oscillator at 40°C, shaken for 1 hour, and then dried in an oven at 105°C for 12 hours, and the dried black powder was ground to 200 mesh to obtain the mixture powder A. 2 parts of 200 mesh coal liquefaction residue and mixture powder A were fully mixed to prepare mixture powder B. The mixture powder B was cold-pressed into a cylinder with a diameter of 7 mm and a height of 10 mm under a pressure of 5 MPa, and a mass of 0.6 g. Put the cylinder in the tube furnace, set the heating rate at 20°C / s, the final temperature of physical activation at 900°C, the constant...
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