An Infrared Spectrophotometric Method for Rapid Determination of Oil in Water Without Using CFC Reagents
A technique for rapid determination of CFCs, applied in the field of infrared spectrometry, to achieve the effect of stable method and rapid determination of targets
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Embodiment 1
[0031] Example 1 (A1750~1735—olive oil mass-volume concentration curve drawing)
[0032] Using olive oil as a benchmark to make a standard curve, measure the peak area value (instrument integration) of each concentration, the results are shown in Table 1:
[0033] Table 1A1750~1735—Olive Oil Mass-Volume Concentration
[0034]
[0035] Infrared spectrum such as figure 1 .
Embodiment 2
[0036] Example 2 (taking olive oil as a reference, verifying the conversion coefficient of animal and vegetable oil molar concentration into mass-volume concentration determined by the molecular weight of animal and vegetable oil)
[0037]a. Take 10 beakers and 10 50mL volumetric flasks, paste the names of animal and vegetable oils (olive oil, soybean oil, palm oil, coconut oil, rapeseed oil), pour a small amount of animal and vegetable oils into the beakers, and pipette each with a micro-syringe Put 5 μL of animal and vegetable oil into a volumetric flask with a corresponding label, use carbon disulfide to make up the volume, and use an oil meter to measure the concentration of each prepared solution. Dilute in an appropriate amount, configure a 50mg / L solution, and measure and confirm the concentration with an oil meter. Table 2 lists the average molecular weight of common animal and vegetable oils and their molecular weight after deducting three O-C=O bonds.
[0038] T...
Embodiment 3
[0045] Prepare mixed hydrocarbons with n-hexadecane, isooctane and benzene at a ratio of 65:25:10 (V / V), and commercially available olive oil, soybean oil, palm oil, coconut oil, rapeseed oil, peanut oil, pork Prepare mixed animal and vegetable oils with oil and tallow according to the ratio of 1:1:1:1:1:1:1 (V / V), pipette 5 μL each of mixed hydrocarbons and mixed animal and vegetable oils into 500ml 0.1M Na 2 S solution, 0.1M sulfuric acid solution and distilled water, set 2 samples for each, fully shake and mix to make simulated (wastewater) water samples. Two samples of each water sample were determined by this method and HJ637-2012, see Table 4. The results show that the water sample pretreatment step of this method is effective, and there is no significant difference between this method and HJ637-2012 method.
[0046] Table 4 Validation of water sample pretreatment steps of this method and comparison with HJ637-2012 test results
[0047]
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