Tobacco extract hydrogen sulfide content measurement method and application thereof
A technology of hydrogen sulfide and extract, which is applied in the field of analytical chemistry, can solve the problems of increasing the back pressure of the chromatographic column, and achieve the effects of good repeatability, fast and simple method, and wide linear range
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Embodiment 1
[0049] The determination sample is jujube extract, accurately weigh 0.5g sample (accurate to 0.1mg) in a 100mL conical flask, accurately add 20mL of 1% sodium hydroxide solution, and use a high-speed homogenizer 10000r / min to extract 2.5 min, take 2.0mL of the extract and pass it through the solid-phase extraction column at a flow rate of 5mL / min, discard the first 0.5mL of the effluent, collect the subsequent 1.0mL of the effluent, and filter the membrane with a 0.45μm aqueous needle Filtered for ion chromatography analysis.
[0050] The mobile phase for ion chromatography analysis is: 1.5mol / L sodium hydroxide-1.0mol / L sodium acetate-2% (volume fraction) ethylenediamine (40:50:10, volume ratio); column temperature: 30°C; flow rate: 1.0mL / min; injection volume: 20μL; detection potential waveform of detector (working electrode: Ag, reference electrode: Ag / AgCl): 0min(-100mV), 0.2min(-100mV), 0.9min(- 100mV), 0.91min(-1000mV), 0.93min(-300mV), 1.0min(-300mV).
[0051] Accordi...
Embodiment 2
[0053] The determination sample is fig extract, accurately weigh 0.5g sample (accurate to 0.1mg) in a 100mL conical flask, accurately add 20mL of 1% sodium hydroxide solution, and use a high-speed homogenizer 10000r / min to extract 2.5 min, take 2.0mL of the extract and pass it through the solid-phase extraction column at a flow rate of 5mL / min, discard the first 0.5mL of the effluent, collect the subsequent 1.0mL of the effluent, and filter the membrane with a 0.45μm aqueous needle Filtered for ion chromatography analysis.
[0054] The mobile phase for ion chromatography analysis is: 1.5mol / L sodium hydroxide-1.0mol / L sodium acetate-2% (volume fraction) ethylenediamine (40:50:10, volume ratio); column temperature: 30°C; flow rate: 1.0mL / min; injection volume: 20μL; detection potential waveform of detector (working electrode: Ag, reference electrode: Ag / AgCl): 0min(-100mV), 0.2min(-100mV), 0.9min(- 100mV), 0.91min(-1000mV), 0.93min(-300mV), 1.0min(-300mV).
[0055] Through th...
Embodiment 3
[0057] The determination sample is tobacco extract, accurately weigh 0.5g sample (accurate to 0.1mg) in a 100mL conical flask, accurately add 20mL of 1% sodium hydroxide solution, and use a high-speed homogenizer 10000r / min to extract 2.5 min, take 2.0mL of the extract and pass it through the solid-phase extraction column at a flow rate of 5mL / min, discard the first 0.5mL of the effluent, collect the subsequent 1.0mL of the effluent, and filter the membrane with a 0.45μm aqueous needle Filtered for ion chromatography analysis.
[0058] The mobile phase for ion chromatography analysis is: 1.5mol / L sodium hydroxide-1.0mol / L sodium acetate-2% (volume fraction) ethylenediamine (40:50:10, volume ratio); column temperature: 30°C; flow rate: 1.0mL / min; injection volume: 20μL; detection potential waveform of detector (working electrode: Ag, reference electrode: Ag / AgCl): 0min(-100mV), 0.2min(-100mV), 0.9min(- 100mV), 0.91min(-1000mV), 0.93min(-300mV), 1.0min(-300mV).
[0059] Accord...
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