A kind of solid-phase extraction removes the method for n-paraffin in oil product
A technology for n-alkanes and oil products, which is applied in the preparation of test samples, instruments, measuring devices, etc., can solve the problems of complicated process and long time consumption, and achieve the effect of short time consumption, high recovery rate and high purity
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example 1
[0036] (1) Preparation of urea stationary phase
[0037] Dissolve 10g of urea in 200mL of isopropanol. After the urea is completely dissolved, add 1g of silica gel to it at 65°C, and ultrasonically treat it for 15 minutes to load the urea on the silica gel. Cool naturally to 25°C, and then cool down to 0-5°C. Place at low temperature for 12 hours, evaporate the solvent to dryness, and dry the obtained solid at 80°C for 15 minutes to obtain a stationary phase.
[0038] (2) Removal of n-alkanes in oil products
[0039] Take 4g of the stationary phase prepared in step (1) and load it into a solid-phase extraction column, add 75 μL of paraffin-based straight-run diesel oil sample to the solid-phase extraction column at 25 ° C, then add 800 μL of isopropanol as an activator, and let it stand for 5 minutes , add 2mL of n-hexane and let it stand for 10 minutes to dissolve the non-normal alkanes not complexed by urea in the solid phase extraction column. Then wash the solid-phase ex...
example 2
[0041] Remove the n-paraffins in the paraffin-based straight-run diesel oil according to the method of example 1, the difference is that in (1) step, 10g urea is dissolved in 200mL isopropanol, 30g silica gel is added thereto, after loading, drying have a stationary phase. (2) In step (2), the stationary phase loaded into the solid phase extraction column is 4 g, and then 100 μL of paraffin-based straight-run diesel oil sample and 1050 μL of isopropanol are added successively as an activator, and 2 mL of n-hexane is added, left to stand for 10 minutes, and 6 mL of n-hexane The eluate was obtained by washing the alkane three times. The purity of the non-normal paraffin component was measured to be 98.15% by mass, and the recovery rate of the non-normal paraffin was 92.34% by mass.
example 3
[0043] Remove normal paraffins in paraffin-based straight-run diesel oil according to the method of Example 1, the difference is that in (1) step, 1g urea is dissolved in 20mL isopropanol, 10g silica gel is added thereto, after loading, drying have a stationary phase. (2) In step (2), the stationary phase loaded into the solid-phase extraction column is 4 g, and then 50 μL of paraffin-based straight-run diesel oil sample and 500 μL of isopropanol are added successively as an activator, 2 mL of n-hexane is added, and left standing for 10 minutes. The alkane was washed three times to obtain an eluent, and the purity of the non-normal paraffin component was measured to be 98.13% by mass, and the recovery rate of the non-normal paraffin was 89.82% by mass.
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