A kind of organosilicon separating gel and its preparation method and application
A silicone and separation gel technology, applied in material inspection products, biological testing, etc., can solve problems such as the impact of test results, achieve good physiological inertia, reduce medical waste, and reduce the chance of virus transmission.
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Embodiment 1
[0028] Take 25 parts of 350cP, 40 parts of 10000cP, 10 parts of 10000000cP linear silicone polymer, 5 parts of 100cP hydroxyl silicone oil, 20 parts of fumed silica treated with hexamethyldisilazane, 1 part of silane joint agent. After mixing the above raw materials evenly, raise the temperature to 60°C and keep it warm for 9 hours, then raise the temperature to 180°C, remove low molecules under negative pressure for 1 hour, control the vacuum degree at -0.09mpa, and obtain the separating gel after cooling. When testing, add about 1.5g of separation gel to the prepared blood collection tube, add blood into the blood collection tube, centrifuge at 2000G for 5min after coagulation, after separation, the separation gel is between serum and plasma, put it upside down, and lay it flat Serum and plasma can no longer be mixed.
Embodiment 2
[0030] Take 10 parts of 50cP, 30 parts of 1000cP, 30 parts of 10000000cP linear silicone polymer, 7 parts of 100cP hydroxyl silicone oil, and 18 parts of fumed silica treated with hexamethyldisilazane and methylchlorosilane for hydrophobic treatment , 3 parts of silane coupling agent. After the above raw materials were mixed evenly, the temperature was raised to 90°C for 11 hours, and then the temperature was raised to 155°C, and the low molecular weight was removed by negative pressure for 4 hours. The vacuum degree was controlled at -0.09mpa, and the separation gel was obtained after cooling. When testing, add about 1.5g of separation gel to the prepared blood collection tube, add blood into the blood collection tube, centrifuge at 1500G for 10 minutes after coagulation, after separation, the separation gel is between serum and plasma, put it upside down, and lay it flat Serum and plasma can no longer be mixed.
Embodiment 3
[0032]Take 50 parts of 1000cp, 19 parts of 10000000cp linear silicone polymer, 15 parts of 100cp hydroxyl silicone oil, and 15 parts of hydrophobization with hexamethyldisilazane, tetramethyldivinyldisilazane and methylchlorosilane Treated fumed silica, 6 parts of silane coupling agent. After the above raw materials were mixed evenly, the temperature was raised to 116°C for 5 hours, and then the temperature was raised to 120°C, and the low molecular weight was removed for 6 hours under negative pressure. The vacuum degree was controlled at -0.09mpa, and the separation gel was obtained after cooling. When testing, add about 1.5g of separation gel to the prepared blood collection tube, add blood into the blood collection tube, centrifuge at 1000G for 5min after coagulation, after separation, the separation gel is between serum and plasma, put it upside down, and lay it flat Serum and plasma can no longer be mixed.
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