Preparation method of electrochemically reduced graphene oxide solid-phase microextraction fibers
A technology for extracting fiber and graphene, applied in scientific instruments, measuring devices, instruments, etc., can solve the problems of weak coating stability and poor reproducibility, and achieve strong adsorption capacity, good thermal and chemical stability, Environmentally friendly effect
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Embodiment 1
[0049] Embodiment 1: the preparation of solid phase microextraction fiber
[0050] (1) Preparation of graphene oxide electrolyte: ultrasonically disperse 30 mg of graphene oxide powder in 10 mL of distilled water to obtain a graphene oxide aqueous solution with a concentration of 3 mg / mL, and add 0.1225 g of NaClO to the dispersion 4 , NaClO 4The concentration is 0.1mol / L, and the graphene oxide electrolyte is obtained after mixing evenly.
[0051] (2) Electrochemical deposition: corrode the lower end 2 cm of the stainless steel wire with aqua regia for 15 minutes, wash it with distilled water, and use it as a working electrode for later use. A CHI660C electrochemical workstation was used, the corroded stainless steel wire was used as the working electrode, the saturated calomel electrode was used as the reference electrode, and the platinum electrode was used as the counter electrode. Using the constant potential method, apply a voltage of -1.2V and keep it for 200-600 seco...
Embodiment 2
[0057] Embodiment 2: Optimization of solid-phase microextraction conditions
[0058] In this experiment, the conditions of solid-phase microextraction were optimized.
[0059] Add benzo[a]pyrene standard working solution to the barbecue supernatant, dilute to 10mL with distilled water, so that the concentration of benzo[a]pyrene is 50ng / mL. Different extraction temperature (40, 50, 60, 70, 80°C), extraction time (10, 20, 30, 40, 50min), stirring rate (100, 300, 500, 700, 900rpm) and desorption time ( 1, 2, 3, 4, 5min) such as Figure 7 , Figure 8 , Figure 9 , Figure 10 As shown, the conditions for a better enrichment and extraction effect are: 70°C as the extraction temperature, 30 min as the extraction time, a stirring rate of 700 rpm, and a desorption time of 4 min.
Embodiment 3
[0060] Example 3: SPME-GC enrichment detection of benzo[a]pyrene in barbecue
[0061] (1) Preparation of standard solution
[0062] Dissolve 1 mg of benzo[a]pyrene standard powder in 10 mL of acetone to prepare a 100 mg / L benzo[a]pyrene stock solution, and dilute the stock solution to 10 mg / L as an intermediate solution. The concentration of the standard curve working solution is 0.05ng / mL, 0.1ng / mL, 0.5ng / mL, 1ng / mL, 5ng / mL, 10ng / mL, 100ng / mL, 200ng / mL.
[0063] (2) Sample pretreatment
[0064] Accurately weigh 2g of roast meat into a centrifuge tube, add 5mL of acetone, ultrasonically extract for 40min, centrifuge at 10000rpm for 10min, and take the supernatant; add 5mL of acetone again, repeat the ultrasonication and centrifugation operations, and combine the supernatant twice.
[0065] (3) SPME combined with GC
[0066] Dilute 50 μL of barbecue supernatant with distilled water into a 10 mL extraction vial, put a stirring bar, insert self-made solid-phase microextraction...
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