Method for determining content of hydrogen peroxide by determining concentration of oxygen
A technology for hydrogen peroxide and oxygen concentration, which is used in measuring devices, instruments, scientific instruments, etc., can solve the problems of insignificant color change at the end point, many interference factors, low sensitivity, etc., and achieves short measurement process time and strong anti-interference ability. , the effect of high sensitivity
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Embodiment 1
[0033] The mensuration of hydrogen peroxide content in the urea peroxide of embodiment 1
[0034] (1) Preparation of hydrogen peroxide standard solution: Accurately measure 2.0mL of 30% hydrogen peroxide solution by mass percentage, add deionized water to dilute to 100mL, and then carry out chemical calibration according to the national standard GB6684-2002.
[0035] (2) Preparation of enzyme solution: Accurately weigh 0.4g of catalase, add phosphate buffer to dissolve, and then dilute to 100mL.
[0036] (3) Establish a standard curve: Add 3.0mL enzyme solution to a series of headspace vials, seal the vials, and then add 0, 0.1, 0.25, 0.5, 0.75, 1.0 , 1.5mL hydrogen peroxide standard solution, put the sample bottle in a water bath, and after reacting at 37°C for 5 minutes, place it on the sample stage, and then perform headspace-gas chromatography detection, and obtain the peak area of the oxygen signal The corresponding relationship between the amount of hydrogen peroxide ...
Embodiment 2
[0041] The mensuration of residual hydrogen peroxide content in the hydrogen peroxide bleaching waste liquor of embodiment 2
[0042] (1) Preparation of hydrogen peroxide standard solution: Accurately measure 2.0mL of 30% hydrogen peroxide solution by mass percentage, add deionized water to dilute to 100mL, and then carry out chemical calibration according to the national standard GB6684-2002.
[0043] (2) Preparation of enzyme solution: Accurately weigh 0.4g of catalase, add phosphate buffer to dissolve, and then dilute to 100mL.
[0044] (3) Establish a standard curve: Add 3.0mL enzyme solution to a series of headspace vials, seal the vials, and then add 0, 0.1, 0.25, 0.5, 0.75, 1.0 , 1.5mL hydrogen peroxide standard solution, put the sample bottle in a water bath, and after reacting at 37°C for 5 minutes, place it on the sample stage, and then perform headspace-gas chromatography detection, and obtain the peak area of the oxygen signal The corresponding relationship betw...
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