Method for simultaneously measuring trivalent chromium and hexavalent chromium in water samples by aid of low-pressure ion chromatograms and inductively coupled plasma mass spectra in combination manner
A low-pressure ion chromatography and inductive coupling technology, applied in the field of detection and analysis of environmental water bodies, can solve problems such as the need for improvement in analysis sensitivity, inability to be used for direct detection, and human injury, and achieve wide linear range, low detection limit, and improved sensitivity Effect
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Embodiment 1
[0028] In the present embodiment, the standard sample is tested to investigate the precision, linear range and detection limit of the method of the present invention, the steps are as follows:
[0029] 1. Preparation of standard samples
[0030] (1) Preparation of Cr(Ⅲ) standard stock solution: Accurately weigh Cr(NO 3 ) 3 9H 2 O0.7692g is placed in the beaker, after dissolving with deionized water, transfer it to a 100mL volumetric flask, and set the volume to 100mL for subsequent use with deionized water to obtain a Cr(Ⅲ) standard stock of 1000.00mg / L with a Cr(Ⅲ) concentration liquid.
[0031] (2) Cr(Ⅵ) standard stock solution: accurately weigh K 2 Cr2 o 7 Put 0.0270g in a beaker, dissolve it with deionized water, transfer it to a 100mL volumetric flask, and set the volume to 100mL with deionized water for later use, to obtain a Cr(Ⅵ) standard stock solution with a Cr(Ⅵ) concentration of 1000.00 mg / L .
[0032] (3) Use the standard stock solution and deionized water ...
Embodiment 2
[0048] In this embodiment, the analysis and determination of the tannery wastewater sample is carried out to investigate the effect of the method of the present invention on simultaneously determining trivalent chromium and hexavalent chromium in the water sample.
[0049] 1. Sample Preparation
[0050] Three samples of tannery wastewater were collected, respectively numbered as 1# sample, 2# sample and 3# sample. After each sample was collected, it was gravity settled for 1 hour, and the supernatant was taken for direct analysis.
[0051] 2. Preparation of eluent E
[0052] 20gNaNO 3 Put it in a beaker, dissolve it with deionized water, transfer it to a 1000mL volumetric flask, and dilute to 1000mL with deionized water.
[0053] 3. Sample spectrum drawing
[0054] use figure 1 and figure 2 The analyzers designed for the process flow shown were tested, where figure 1 is the sample injection state, figure 2 For analysis state, this analytical instrument comprises low-p...
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