Method for removing cesium ions in blood
A cesium ion and blood technology, which is applied in the field of blood purification and nuclear medicine emergency, can solve the problem that the flame atomic absorption spectrophotometer cannot meet the detection requirements and takes a long time (it takes days to weeks, and it is not suitable for cesium ion removal) and other issues to achieve the effect of improving biocompatibility, preventing sedimentation, preventing agglomeration and sedimentation
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Embodiment 1
[0033] FeCl 3 ·6H 2 O (1.0g, 3.7mmol) was dissolved in 40mL of ethylene glycol, and then polyethylene glycol (0.1g, M n =2000g / mol), sodium acetate (0.8g, 9.7mmol) and sodium dodecylsulfonate (0.8g, 2.3mmol), then 5mL K 3 [Fe(CN) 6 ]·3H 2 O (0.4 g, 1.0 mmol) aqueous solution was added to the above mixture, and the stirring was continued until the system was uniform, and finally concentrated hydrochloric acid (0.6 mL, 37.5 wt %) was added. The mixture was then transferred to a stainless steel reactor with a polytetrafluoroethylene liner, heated to 180 °C and maintained for 6 hours. Then it was cooled to room temperature, washed once with ethanol, then washed once with water, and finally washed once with ethanol, and vacuum-dried to constant weight to obtain the magnetic Prussian blue adsorbent. Such as figure 1 as shown, figure 1 (A) is the dispersion state diagram of the magnetic Prussian blue nanoparticles in water. In water, the adsorbent dispersion liquid is uniform ...
Embodiment 2
[0044] Fe(NO 3 ) 3 9H 2 O (1.0g, 2.5mmol) was dissolved in 40mL of ethylene glycol, and then polyethylene glycol (0.1g, M n =2000g / mol), sodium acetate (0.8g, 9.7mmol) and sodium dodecylsulfonate (0.8g, 2.3mmol), then 5mL K 3 [Fe(CN) 6 ]·3H 2 O (0.4 g, 1.0 mmol) aqueous solution was added to the above mixture, and the stirring was continued until the system was uniform, and finally sulfuric acid (0.6 mL, 5 mol / L) was added. The mixture was then transferred into a stainless steel reactor with a polytetrafluoroethylene liner, heated to 200 °C and maintained for 6 hours. Then it was cooled to room temperature, washed once with ethanol, then washed once with water, and finally washed once with ethanol, and vacuum-dried to constant weight to obtain the magnetic Prussian blue adsorbent.
[0045] Disperse the above-prepared adsorbent in the blood. After the adsorption is balanced, the adsorbent is sucked out from the blood with a magnet, and 1 mL of blood is taken before and af...
Embodiment 3
[0048] Fe(SO 4 ) 3 ·5H 2 O (1.5g, 3.0mmol) was dissolved in 40mL of ethylene glycol, and then polyethylene glycol (0.1g, M n =2000g / mol), sodium acetate (0.8g, 9.7mmol) and sodium dodecylbenzenesulfonate (0.8g, 2.3mmol), then 5mL of Na 3 [Fe(CN) 6 ]·H 2 O (0.4g, 1.3mmol) aqueous solution was added to the above mixture, and the stirring was continued until the system was uniform, and finally sulfuric acid (0.6mL, 5mol / L) was added. The mixture was then transferred to a stainless steel reactor with a polytetrafluoroethylene liner, heated to 185 °C and maintained for 6 hours. Then it was cooled to room temperature, washed once with ethanol, then washed once with water, and finally washed once with ethanol, and vacuum-dried to constant weight to obtain the magnetic Prussian blue adsorbent.
[0049] Disperse the above-prepared adsorbent in the blood. After the adsorption is balanced, the adsorbent is sucked out from the blood with a magnet, and 1 mL of blood is taken before a...
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