Method for identifying tea oil based on 3D fluorescence spectrum technology
A fluorescence spectrum technology, tea oil technology, which is applied in the field of identification of adulterated tea oil and camellia oil based on 3D fluorescence spectrum, can solve the problems of inability to detect in real time, high detection cost, cumbersome methylation, etc.
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Embodiment 1
[0018] (1) Sample pretreatment: Take 20 mL of the tea oil sample to be tested, add an equal volume of dichloromethane and mix evenly, place it in a separatory funnel, use 30% ethanol aqueous solution as the extraction agent for conventional extraction, separate, and concentrate the supernatant to 4mL, as the sample to be tested for 3D fluorescence spectroscopy;
[0019] (2) 3D fluorescence spectrum detection: detection instrument: PDA; fluorescence spectrum parameters are detection excitation wavelength is 380nm, emission wavelength is 430nm, slit width is 4nm, step size is 4nm;
[0020] (3) Test results and judgment: Compared with the 3D fluorescence spectrum of genuine camellia oil, there is no significant difference in the overall fluorescence spectrum morphology, characteristic excitation / emission peaks and fluorescence intensity. Determined as camellia oil.
Embodiment 2
[0022] (1) Sample pretreatment: take 20mL of the tea oil sample to be tested, add 40mL of dichloromethane and mix evenly, place it in a separatory funnel, use 50% ethanol aqueous solution as the extraction agent for conventional extraction, separate, and concentrate the supernatant to 4mL , as a sample to be tested for 3D fluorescence spectroscopy;
[0023] (2) 3D fluorescence spectrum detection: detection instrument: PDA; fluorescence spectrum parameters are detection excitation wavelength of 400 nm, emission wavelength of 450 nm, slit width of 4 nm, and step size of 4 nm;
[0024] (3) Test results and judgment: Compared with the 3D fluorescence spectrum of genuine camellia oil, there is no significant difference in the overall fluorescence spectrum morphology, characteristic excitation / emission peaks and fluorescence intensity. Determined as camellia oil.
Embodiment 3
[0026] (1) Sample pretreatment: Take 20mL of the sample to be tested, add 60mL of dichloromethane and mix evenly, then place it in a separatory funnel; use 60% ethanol aqueous solution as the extraction agent for conventional extraction and separation, and concentrate the supernatant to 4mL, as 3D fluorescence spectrum of the sample to be tested;
[0027] (2) 3D fluorescence spectrum detection: detection instrument: PDA; fluorescence spectrum parameters are detection excitation wavelength of 400 nm, emission wavelength of 450 nm, slit width of 4 nm, and step size of 4 nm;
[0028] (3) Test results and judgment: Compared with the 3D fluorescence spectrum of genuine camellia oil, there is no significant difference in the overall fluorescence spectrum morphology, characteristic excitation / emission peaks and fluorescence intensity. Determined as camellia oil.
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