A material with tunable wave-absorbing properties and its preparation method
A wave-absorbing performance and tuning technology, applied in the field of preparation of the material, can solve the problems of single nature, complicated preparation process, uncontrollable wave-absorbing performance, etc., and achieve the effects of stable sample performance, simple preparation method and simple operation.
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Embodiment 1
[0036] Preparation of two-dimensional carbon-based supported cerium oxide nanocomposites
[0037] Dissolve 0.4 g (3.2 mmol) of melamine in 100 mL of water at 80°C. 1.0g F127 (poloxamer, purchased from Macklin, P822479-50g, polyethylene glycol-polypropylene glycol-polyethylene glycol triblock copolymer surfactant, H(OCH 2 CH 2 ) x (OCH 2 CHCH 3 ) y (OCH 2 CH 2 ) z OH, average molecular weight Mn~13,000) was added into 40mL of water, placed in a 40°C water bath, and stirred for 1h. Then add 0.3g (0.7mmol) Ce(NO 3 ) 3 ·6H 2 O, stirred for 2h. The above two solutions were mixed and stirred in a water bath at 60°C until evaporated to dryness. The evaporated solid was placed in a tube furnace and sintered under the protection of nitrogen. The sintering procedure was as follows: after heating up from 20 °C to 350 °C at a heating rate of 1 °C / min, the temperature was kept for 3 h; After the heating rate was raised from 350°C to 850°C, the temperature was kept for 2 hours...
Embodiment 2
[0039] Preparation of two-dimensional carbon-based supported cerium oxide nanocomposites with different loadings
[0040] Add 6 parts of 1.0g F127 to 6 containers filled with 40mL water respectively, place in a water bath at 40°C, and stir for 1h. Then 0.05g, 0.10g, 0.20g, 0.50g, 0.70g and 0.90g of Ce(NO 3 ) 3 ·6H 2 O, stirred for 2h. Dissolve 6 parts of 0.4g melamine in 6 containers filled with 100mL of 80°C water respectively. Mix the obtained 6 parts of cerium nitrate solution with 6 parts of melamine solution respectively, and stir in a water bath at 60° C. until evaporated to dryness. The evaporated solid was placed in a tube furnace and sintered under the protection of nitrogen. The sintering procedure was as follows: after heating up from 20 °C to 350 °C at a heating rate of 1 °C / min, the temperature was kept for 3 h; After the heating rate was raised from 350°C to 850°C, the temperature was kept for 2 hours. After natural cooling to room temperature, the obtained...
Embodiment 3
[0042] Preparation of two-dimensional carbon-based supported lanthanide rare earth oxide nanocomposites with different loading types
[0043] Add 13 parts of 1.0g F127 to 13 containers filled with 40mL of water respectively, place in a water bath at 40°C, and stir for 1h. Then, hydrated rare earth nitrates (in turn, hexahydrated lanthanum nitrate La(NO 3 ) 3 ·6H 2 O), cerium nitrate hexahydrate (Ce(NO 3 ) 3 ·6H 2 O), praseodymium nitrate hexahydrate (Pr(NO 3 ) 3 ·6H 2 O), neodymium nitrate hexahydrate (Nd(NO 3 ) 3 ·6H 2 O), samarium nitrate hexahydrate (Sm(NO 3 ) 3 ·6H 2 O), europium nitrate hexahydrate (Eu(NO 3 ) 3 ·6H 2 O), gadolinium nitrate hexahydrate (Gd(NO 3 ) 3 ·6H 2 O), terbium nitrate hexahydrate (Tb(NO 3 ) 3 ·6H 2 O), dysprosium nitrate hexahydrate (Dy(NO 3 ) 3 ·6H 2 O), erbium nitrate hexahydrate (Er(NO 3 ) 3 ·6H 2 O), thulium nitrate hexahydrate (Tm(NO 3 ) 3 ·6H 2 O), ytterbium nitrate pentahydrate (Yb(NO 3 ) 3 ·5H 2 O) and lantha...
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